Professional Documents
Culture Documents
Performance
Impaired performance
information into memory because of strong anxiety
Positive Negative
punishment punishment of information is often based on priming
Increasing attention
interconnected nodes of the semantic network. and interest
Weak
Recognition of information is stronger than recall. Low High
Arousal
Somatic symptom
• Drive and theory:
reduction related individuals
disorders act • SOCIAL INTERACTION
PSYCHOLOGICAL DISORDERS
• Cultural relativism: studying social groups and
to relievesymptom
• Somatic internal states of tension
disorder: at least one cultures on their own terms
• somatic
Maslow’ssymptom,
hierarchywhich
of needs:
mayprioritizes
or may notneeds
be Elementsand
Diagnostic of Social Interaction
Statistical Manual of Mental Disorders Anxiety disorders
• Discrimination: when prejudicial attitudes
into five
linked categories:
to an underlyingphysiological needs that
medical condition, (DSM): the guide
• Status: by which
a position in most psychological
society used to disorders cause differences
• Generalized anxietyindisorder:
treatment of a
constant
(highestdisproportionate
causes priority), safety and security, love and
concern are characterized, described,
classify individuals. Can and diagnosed.
be ascribed disproportionate
group and persistent worry
belonging, self-esteem, and self-actualization (involuntarily assigned), achieved
• Illness anxiety disorder: preoccupation with
Types(voluntarily
of Psychological SOCIAL STRUCTURE
• Specific AND DEMOGRAPHICS
phobias: irrational fears of specific
(lowestor
having priority)
coming down with a serious earned), or Disorders
master (primary objects
medical condition Schizophrenia:
identity) psychotic disorder characterized by • Social anxiety disorder: anxiety due to social
Emotion
• Conversion disorder: unexplained symptoms
distortions
• Role:of setreality and disturbances
of beliefs, in content
values, and norms that Sociology: Theories situations
or performance and Institutions
and form of thought,
define perception,ofand
the expectations behavior.
a certain
Seven affecting
universalmotor or sensory
emotions: function
happiness, sadness, •• Agoraphobia:
Functionalism:fear focuses on the
of places function and
or situations
Positive symptoms include hallucinations, delusions,
status relationships
contempt, surprise, fear, disgust, anger where it is hard of each
for an component
individual to escapeof
Personality disorders and •disorganized
Group: twothought
or moreand behavior.with
individuals Negative
similar society
Theories of emotion: • Panic disorder: recurrent attacks of intense,
Patterns of inflexible, maladaptive behavior that symptoms include disturbance
characteristics who share of affect
a senseand of avolition.
unity • overwhelming
Conflict theory: focuses on how power
fear and sympathetic nervous
cause distress or impaired functioning • Network:
Depressive disorders observable pattern of social system activity
differentials arewith no clear
created and stimulus.
how theyIt may
First Second lead to agoraphobia.
relationships
Major depressive between
disorder: individuals
contains at leastor maintain order
• Cluster A (odd, eccentric,
Theory “weird”): response
response
groups
one major depressive episode • Symbolic interactionism:
Obsessive–compulsive the study of
disorder: obsessions
paranoid, schizotypal, schizoid
James–Lange Nervous Conscious Organization:
• Pervasive group with a structure how individuals
(persistent, interact through
intrusive thoughts a shared
and impulses) and
• Cluster B (dramatic, emotional, erratic, “wild”): depressive disorder: a depressed
system emotion and culture
mood (eitherdesigned
dysthymiato achieve
or major depression) understanding
compulsions (repetitiveof words, gestures,
tasks that relieve and other
tension but
antisocial, borderline, histrionic, narcissistic
arousal specific
for at least two years symbols impairment)
cause significant
• Cluster C (anxious, fearful, “worried”):
Cannon–Bard
avoidant, dependent, Nervous Action
obsessive–compulsive Seasonalgoals; exists
affective outsidethe
disorder: of each individual’s
colloquial Body• dysmorphic
Social constructionism: explores
disorder: unrealistic how
negative
membership within the organization
STIMULUS
(homeostasis)
diversity Type Inventory
• Social capital: the investment people
2. Resistance of the surroundings or social context
• Subculture: a group that stagedistinguishes itself • Eysenck’s three major
make in society traits:
in return psychoticism,
for economic or
• Correspondent inference theory: describes
from the primary culture to which it belongs extraversion,
collective neuroticism
rewards
breakdown attributions made by observing the
(burnout) Trait theorists’
intentionalBig Five: openness,
(especially unexpected) • Social reproduction: the passing on of
Socialization Time
Erikson’s stages of
behaviors psychosocial
performed development
by another person conscientiousness,
social extraversion,
inequality, especially poverty, to other
• Socialization: the process of developing agreeableness, and neuroticism (OCEAN)
generations
IDENTITY AND PERSONALITY •• Stem
Fundamental attribution
from conflicts that error:
are thebias toward
result of decisions
and spreading norms, customs, and beliefs making dispositional attributions rather than • Allport’s
Poverty: three
low SES; in types
basic the US,
of the poverty
traits: line is
cardinal,
we are forced to make about ourselves and the
Self-Conceptboundaries
• Norms: and Identity of acceptable behavior situational attributions the government’s
central, calculation of the
and secondary
environment around us at each phase of our lives
within society minimum income requirements to acquire
• Self-concept: the sum of the ways in which • Stages are trust vs. mistrust, autonomy vs.
• Stigma: extreme disapproval or dislike Stereotypes,
shame andPrejudice, and Discrimination
doubt, initiative vs. guilt, industry
the minimum necessities of life
we describe ourselves: in the present, who we
of a person or group based on • vs.
Stereotypes:
inferiority,attitudes
identityand
vs. impressions that
role confusion,
used to be, and who we might be in the Epidemiology
perceived differences are madevs.
intimacy based on limited
isolation, and superficial
generativity vs.
• future
Identities: individual components of our self- new cases
• Deviance: any violation of norms, rules, or information integrity vs. despair
stagnation,
concept related to the groups to which we Incidence: per time
expectations within a society • Self-fulfilling
• belong
Self-esteem: our evaluation of ourselves Kohlberg’s theory of prophecy: the phenomenon
moral reasoning development population- at risk
• Conformity: changing beliefs or behaviors in of a stereotype creating an expectation of a
• order
Self-efficacy: theadegree
to fit into group orto which
societywe see • Describes the approaches of individuals
particular group, which creates conditions that number of cases(new or old)
ourselves as being capable of a given skill in to resolving moral dilemmas
• Compliance: individuals change behavior lead to confirmation of this stereotype Prevalence: per time
a
given situation •• Six stages are divided into three main
based on the request of others; techniques Stereotype threat: a feeling of anxiety total population
• for
Locus of control: a self-evaluation that refers phases: preconventional, conventional,
gaining compliance include foot-in-the- about confirming a negative stereotypeand
to the door-in-the-face,
way we characterize the influences in Morbidity: the burden or degree of illness associated
door, lowball, and that’s- • postconventional
Prejudice: an irrationally based attitude with a given disease
our lives. Either internal (success or failure is a
not-all prior theory
Vygotsky’s to actual experience
of cultural and biosocial
result of our own
• Obedience: actions)
change or external
in behavior based(success
on a Mortality: deaths caused by a given disease
development
• Ethnocentrism: the practice of making
or failure isfrom
command a result of outside
someone seenfactors)
as an judgmentsdevelopment
• Describes about otherofcultures based
language, on
culture,
authority figure the values
and skills and beliefs of one’s own
culture (in-group vs. out-group)
A LA
I MCAT QUICKSHEETS BIOCHEMISTRY ąr*
NONENZYMATIC PROTEIN FUNCTION BIOSIGNALING
Amino Acids Found in Proteins
AND PROTEIN ANASIRS Ion channels can be used for regulating ion flow
Amino acids have an amino group, c arboxylic acid, a Cellular Functions into or out of a cell. There are three main types of
hydrogen atom, and an R group attached to a central Structural proteins: generally fibrous. Include ion channels: ungated channels, voltage-gated
n-carbon. collagen, elastin, keratin, actin, and tubulin channels, and ligand-gated channels.
H o Motor proteins: capable of force generation through Enzyme-linked receptors participate in cell signaling
a conformational change. Include myosin, through extracellular ligand binding and initiation
ON ^
H OH kinesin, and dynein of second messen er cascades.
R G protein-coupled receptors have a membrane
bound protein associated with a trimeric G protein.
Amino acids are chiral (L), except for glycine; and
have the (S) configuration, except for cysteine. They also initiate second messenger systems.
Side chains determine the chemistry and function of e
amino acids:
• Nonpolar, nonaromatic: glycine, alanine,
valine, leucine, isoleucine, methionine, proline GDP
• Aromatic: tryptophan, phenylalan ine, tyrosine ' •’*°""•"’‹'• ›
• Polar: serine, threonine, asparagine, Binding proteins: bind a specific substrate, either nactive G protein active G protein
glutamine, cysteine to sequester it in the body or hold its concentration
• Negatively charged (acidic): aspartic acid, at steady state
glutamic acid
Cell adhesion molecules (CAMs): bind cells to other
• Positively charged (basic): lysine, arginine, GTP
histidine cells or surfaces. Include cadherins, integrins, and
selectins
Antibodies (or immunoglobulins, Ig): target a
Acid—Base Chemistry of Amino Acids specific antigen, which may be a protein on the
Amino acids are amphoteric. surface of a pathogen (invad ing organism)
GDP
• At low (acid ie) pH: fully protonated or a toxin
• At neutral pH: zwitterion
• At high (basic) pH: fully deprotonated ENZYMES
pt is determined by averaging the pd, values that refer Enzyme Kinetics
to protonation and deprotonation of the zwitterion.
Saturation kinetics: As substrate concentration
increases, the reaction rate also increases until a
Peptide Bond Formation and Hydrolysis maximum value is reached.
Peptide bond formation is a condensation
(dehydration) reaction with a nucleophilic amino
group attacking an electrophilic carbonyl. Peptide
bonds are broken by hydrolysis.
Atone-hañvpa {S)=
H*or 0 H Michaelis—Menten
• Ligases are responsible for joining two large
biomolecules, often of the same type.
• Isomerases catalyze the interconversion of
isomers, including both constitutional and
stereoisomers.
• Lyases catalyze cleavage without the addition
Protein Structure of water and without the transfer of electrons.
Primary structure: linear sequen ce of amino acids The reverse reaction (synthesis) is usually more
biologically important.
Secondary structure: local structure, stabilized by Lineweaver—Burk
hyd rogen bonding • Hydrolases catalyze cleavage with the add ition
of water.
n-helixes • Oxidoreductases catalyze oxidation—reduction
• ,/J-pleated sheets reactions that involve the transfer of electrons.
Tertiary structure: three-dimensional structure • Transferases move a functional group from one
stabilized by hydrophobic interactions, acid—base molecule to another molecule.
interactions (salt bridges), hydrogen bonding, and Enzymes, like all catalysts, lower the activation
disulfide bonds energy necessary for reactions. They do not
H O alter the free energy 6G) or enthalpy (A//l
change that accompanies the reaction nor the
final equilibrium position; rather, they change the Cooperative enzymes show a sigmoidal curve.
|" rate (kinetics) at which equilibrium is reached.
OH
Eukaryotic Chromosome Organization
CH2OH CH2OH CH2OH CH2OH DNA replication is semiconservative: one old parent
D-fructose D-glucose D-galactose D-mannose
DNA is organized into 46 chromosomes in human cells. strand and one new daughter strand is incorporated
Monosaccharides are single carbohydrate units In eukaryotes, DNA is wound around histone proteins into each of the two new DNA
and can undergo three main reactions: molecules. (H2A, H2B, H3, and H4) to form nucleosomes, which leading strand
DNA polymerase III
may be stabilized by another histone protein (H1). 5’
oxidation–reduction, esterification, and glycoside
on leading strand
formation. DNA and its associated histones make up chromatin 3’ ssDNA-binding protein
Sugars with a –H replacing an –OH group are termed Euchromatin is less dense, transcriptionally 5’ 5’
{
Central Dogma: DNA → RNA → proteins A U G C C G U A U G C U A U G C C G U A U G C U
active transport
U A C U A CG G C passive transport
• thymine R
binds
R
Glyceraldehyde-3-phosphate dehydrogenase:
rrepressor
inducer I inducer—repressor
repressor repressor—corepressor
complex binds to
produces NADH
There are three major types of RNA in transcription: R
I complex cannot bind
R to operator—structural
R C R C operator and represses
enzyme synthesis
• 3-phosphoglycerate kinase and
genes are transcribed
message from DNA in the nucleus via inducible system repressible system phosphorylation
transcription of the gene; travels into the
Control of Gene Expression in Eukaryotes Glucokinase/hexokinase, PFK-1, and pyruvate kinase
cytoplasm to be translated
catalyze irreversible reactions.
• Transfer RNA (tRNA): brings in amino acids; Transcription factors search for promoter and
recognizes the codon on the mRNA using enhancer regions in the DNA. The NADH produced in glycolysis is oxidized
its anticodon aerobically by the mitochondrial electron transport
• Promoters are within 25 base pairs of the
chain and anaerobically by cytoplasmic lactate
• Ribosomal RNA (rRNA): makes up much of the transcription start site.
dehydrogenase.
ribosome; enzymatically active • Enhancers are more than 25 base pairs
away from the transcription start site.
++––
Pyruvate Dehydrogenase • Each NADH: 2.5 ATP; 10 NADH form 25 ATP LIPID AND AMINO ACID METABOLISM
• Converts pyruvate to acetyl-CoA. Stimulated by • Each FADH2: 1.5 ATP; 2 FADH2 form 3 ATP
insulin and inhibited by acetyl-CoA. • GTP are converted to ATP. Lipid Transport
• 2 ATP from glycolysis + 2 ATP (GTP) from citric Lipids are transported via chylomicrons, VLDL, IDL,
The Citric Acid Cycle acid cycle + 25 ATP from NADH + 3 ATP from LDL, and HDL.
Takes place in mitochondrial matrix. Main purpose FADH2 = 32 ATP per molecule of glucose
is to oxidize acetyl-CoA to CO2 and generate high- (optimal). 30–32 ATP per molecule of TGL TGL Adipose
energy electron carriers (NADH and FADH2) and GTP. glucose is the commonly accepted range for CE
Chylomicron
CE
Chylomicron
Glucose
energy yield Intestine
(epithelium)
(lymph) (blood)
Li poprotein
Pyruvate Amino acids lipase
Malate
cis-Aconitase It is activated by insulin in the liver and TGL Fatty acids
Isocitrate
block of oligoglucose from one chain and
Malate
dehydrogenase connects it as a branch using an α-1,6 Cholesterol Metabolism
Fumarase NADH CO2
glycosidic link. • Cholesterol may be obtained through dietary
α-Ketoglutarate Glycogenolysis is the breakdown of glycogen
NAD
α-Ketoglutarate using two main enzymes: sources or through synthesis in the liver.
Fumarate
FADH2
NADH
dehydrogenase • The key enzyme in cholesterol biosynthesis is
Succinate • Glycogen phosphorylase, which removes
dehydrogenase FAD CO2
HMG-CoA reductase.
(complex II)
Succinate
GTP GDP + Pi Succinyl-CoA
single glucose 1-phosphate molecules by
breaking α-1,4 glycosidic links. In the liver, Palmitic acid, the only fatty acid that humans can
Succinyl-CoA
synthetase
it is activated by glucagon to prevent low synthesize, is produced in the cytoplasm from
blood sugar. In exercising skeletal muscle, acetyl-CoA transported out of the
it is activated by epinephrine and AMP to mitochondria.
The Electron Transport Chain
provide glucose for the muscle itself. Fatty acid oxidation occurs in the mitochondria,
Takes place on the matrix-facing surface of the inner
• Debranching enzyme, which moves a block of following transport by the carnitine shuttle, via
mitochondrial membrane.
oligoglucose from one branch and connects β-oxidation.
NADH donates electrons to the chain, which are it to the chain using an α-1,4 glycosidic link.
Ketone bodies form (ketogenesis) during a
passed from one complex to the next. Reduction
prolonged starvation state due to excess acetyl-CoA
potentials increase down the chain, until the Gluconeogenesis
in the liver. Ketolysis regenerates acetyl-CoA for use
electrons end up on oxygen, which has the highest Occurs in both the cytoplasm and mitochondria, as an energy source in peripheral tissues.
reduction potential. predominantly in the liver. Most of gluconeogenesis
Step 1 Step 2
is just the reverse of glycolysis, using the same
Protein Catabolism
Cyt c
Cyt c
2H
+
(ox) 2 H+ (ox)
4× Cyt c 2 H+
(red)
Q
1e –
Cyt c
(red)
Q
1e
Cyt c
(red) 4× Cyt c
(ox)
4
eCu enzymes.
Fe-S
centers Q Fe Q QH2 QH2 Fe
Protein digestion occurs primarily in the small
The three irreversible steps of glycolysis must be
Fe-S QH2 QH2
QH2 Q
centers 1 e– 1 e– Fe
Q Q
intestine. Carbon skeletons of amino acids are used
Heme
4 H+ + O2 Cu
Succinate Fumarate + 2 H
+
• Pyruvate carboxylase and PEP carboxykinase body formation. Amino groups are fed into the urea
Complex I Complex II Complex III Complex IV
bypass pyruvate kinase cycle for excretion.
NADH cannot cross the inner mitochondrial • Fructose-1,6-bisphosphatase bypasses
membrane, so must use one of two shuttle phosphofructokinase-1 Glycogen
Insulin Glucagon
synthesis
mechanisms to transfer its electrons to energy • Glucose-6-phosphatase bypasses hexokinase/
carriers in the mitochondrial matrix: the glycerol glucokinase Lipid
Cellular glucose
uptake
Glycogenolysis Stimulates
Inhibits
3-phosphate shuttle or the malate–aspartate synthesis
Lipolysis
Plasma glucose
shuttle.
The Pentose Phosphate Pathway Protein Glucose
Protein
catabolism
synthesis utilization
Oxidative Phosphorylation Occurs in the cytoplasm of most cells, generating Ureagenesis
REPRODUCTION HOMEOSTASIS
Cell Division Four Stages of Early Development Osmoregulation
• G : cell increases its organelles and cytoplasm Cteavage: mitotic divisions • Filtration at the glomerulus. Filtrate (fluid and
• S: DNA replication Implantation: embryo implant s during blastula small solutes) passes through. Passive
• G2. same as G stage • Secretion of acids, bases, and ions from
• M: the cell divides in Gastrulation: ectoderm, endoderm, and interstitial fluid to filtrate. Maintains pH, [K*]
• two Mitosis = PMAT mesoderm form and [waste]. Passive and Active
• Meiosis = PMAT x 2 Neurutation: germ layers develop a nervous system • Reabsorption: essential substances and
Mitosis isis blastula water flow from filtrate to blood. Enabled by
(blastocyst) füastocoel çq,qe,y osmolarity gradient and selective permeability
of the walls. Passive and Active
e
archenteron
Aldosterone
endofierm
• Stimulates Na* reabsorption, K* and H*
Ectodem Nervous system, epidermis, lens secretion, increasing water reabsorption,
“Attract”oderm of eye, inner ear blood volume, and blood pressure
Endoderm Lining of digestive tract, lungs, • Secreted from adrenal cortex
“Endernal" organs liver and pancreas • Is regulated by the renin—angiotensin—
Mesoderm Muscles, skeleton, circulatory aldosterone system
“Means"oderm system, gonads, kidney
ADH (Vasopressin)
’actve vansooRatoo
ENDOCRINE SYSTEM
Direct hormones directly stimulate organs; tropic hormones stimulate other glands. Four Stages of Menstrual Cycle:
Mechanisms of hormone action: peptides act via second messengers and steroids act via hormone/receptor
1. Follicular: FSH causes growth of a follicle
binding to DNA. Amino acid-derivative hormones may do either.
2. Ovulation: LH causes follicle to release egg
Hormone Source Action 3. Luteal: corpus luteum forms
Follicle-stimulating (FSH) Stimulates follicle maturation; spermatogenesis 4. Menstruation: endometrial lining sheds
Luteinizing (LH) Stimulates ovulation; testosterone synthesis day 14 ruptures-egg released
Hypothalamus LH surge follicle
Stimulates adrenal cortex to make and secrete (ovulation)
Adrenocorticotropic (ACTH) glucocorticoids
day 0 LH
no pregnancy corpus luteum atrophies
GnRH corpus luteum
(inhibition stops, cycle
Anterior pituitary Stimulates the thyroid to produce thyroid starts anew)
Thyroid-stimulating (TSH) hormones pituitary
progesterone
zygote
early in cycle
Prolactin Stimulates milk production and secretion (prevents multiple
later in maintains
FSH cycle uterine wall hCG
Endorphins Inhibits the perception of pain in the brain egg development)
(LH analog)
dendrites
synaptic cleft.
• Neurotransmitter binds to receptors on
action
the postsynaptic membrane, triggering K
axon
+ potential
Relaxation:
depolarization. +
–
+
–
–
+
–
+
+
–
+
–
+
– –
+
Na– –+ –
+ –+ +
– +
– +
– +
– • Ca2+ is pumped back into the
sarcoplasmic reticulum.
+
K
action
+
K + potential Bone Formation and Remodeling
+ + + + – – – –
• Osteoblast: builds bone
Osteoclast: breaks down bone
– – – – + + + +
+
Na– +
– –+ –+ –
+ –+ –+ –+ • Reformation: inorganic ions are absorbed from
K+
the blood for use in bone
• Degradation (resorption): inorganic ions are
released into the blood
CIRCULATION RESPIRATION IMMUNE SYSTEM
Circulatory Pathway Through Heart Gas Exchange • The body distinguishes between “self”
and “nonself” (antigens).
pulmonary veins • Exchange
occurs across
L. pulmonary artery trachea Humoral Immunity (Specific Defense)
aorta the thin
L. atrium
walls of bronchus B-lymphocytes
mitral valve
R. pulmonary artery
• alveoli. memory cells plasma cells make and
L. ventricle
Deoxygenated remember antigen, release antibodies (IgG,
superior vena cava blood speed up secondary IgA, IgM, IgD, IgE),
R. atrium
inferior vena cava enters the response which induce antigen
bronchiole
tricuspid Valve R. ventricle
septum
pulmonary phagocytosis
capillaries • Active imumunity: antibodies are produced
Superior and inferior vena cava → right atrium that surround during an immune response
→ right ventricle → pulmonary arteries → • the alveoli. diaphragm • Passive immunity: antibodies produced by
lungs→ pulmonary veins → left atrium → left O2 from the alveoli one organism are transferred to another
ventricle → aorta → body inhaled air organism
Three portal systems: Blood travels through an extra diffuses down
capillary bed before returning to the heart. its gradient
into the capillaries, where it binds with Cell-Mediated Immunity (Specific Defense)
• Liver (hepatic), kidney, and brain hemoglobin and returns to the heart.
(hypophyseal) • CO from the tissues diffuses from the T-lymphocytes
2
capillaries to the alveoli, and is exhaled. cytotoxic T-cells
Fetal Circulation destroy cells directly
suppressor T-cells
Fetal Respiration
• Foramen ovale: connects right and left helper T-cells regulate B- and T-cells
• Fetal hemoglobin has a higher affinity for
• atria Ductus arteriosus: connects pulmonary activate B- and T-cells to decrease anti-antigen
oxygen than adult hemoglobin.
artery to aorta. Along with foramen ovale, and macrophages by activity
shunts blood away from lungs • Gas and nutrient exchanges occur across the secreting lymphokines
placenta. memory cells
• Ductus venosus: connects umbilical vein
to inferior vena cava, connecting umbilical
circulation to central circulation DIGESTION Nonspecific Immune Response
Includes skin, passages lined with cilia,
Blood Components macrophages, inflammatory response, and interferons
(proteins that help prevent the spread of a virus)
Plasma: aqueous mix of nutrients, wastes,
hormones, blood proteins, gases, and salts
Lymphatic System
Erythrocytes (red blood cells): carry oxygen
pharynx • Lymph vessels meet at the thoracic duct in the
• Hemoglobin: four subunits carry O2 and CO2 oral cavity
upper chest and neck, draining into the left
.
Iron controls binding and releasing. tongue
subclavian vein of the cardiovascular system.
trachea
• Oxygen–hemoglobin dissociation: • Vessels carry lymph (excess interstitial
esophagus fluid), and lacteals collect fats by absorbing
Factors leading to right 100
80
P
2 20
25
gallbladder
pancreas Lipid Digestion
• O2 release to curve shifts to the RIGHT
colon
tissues
pH shifts DOWN
0
20 40 60 80 100 duodenum
• When chyme is present, the duodenum
enhanced + P (mmHg) small intestine secretes the hormone cholecystokinin (CCK) into
when H O2
may enter
8 4 cycle
12
• Acellular structures of double- or single- progeny assembly replication of
viral chromosome
lytic cycle
prophage
stranded DNA or RNA in a protein coat
Patterns of • Lytic cycle: virus kills the host cell
Inheritance • Lysogenic cycle: virus enters host genome
• Autosomal recessive: skips generations
• Autosomal dominant: appears in every DATA ANALYSIS
generation
• X-linked (sex-linked): no male-to-male A researcher performed the following experiments in Experiment 2
transmission, and more males are affected order to investigate the metabolism of two
The two strains were incubated in the same manner
different strains of bacteria, Strain 1 and Strain 2.
as in Experiment 1. Two 100 mL portions of agar were
EVOLUTION poured into two beakers, which were maintained at
Experiment 1 43˚C. Next, 0.2 mL of broth culture from Strain 1 was
• When frequencies are stable, the population Strains 1 and 2 were incubated in separate broth pipetted into the first beaker, and 0.2 mL of broth
is in Hardy–Weinberg equilibrium: no cultures for 24 hours at 37˚C. A sample of each culture from Strain 2 was pipetted into the second
mutations, large population, random culture was streaked onto three different plates— beaker. The agar was swirled around to distribute
mating, no migration, and equal A, B, and C—each containing a different starch–agar the bacteria evenly through the media, and then
reproductive success medium; the plates were then incubated for poured onto plates. These plates were incubated
p + q = 1; p 2 + 2pq + q2
+++
another 48 hours at 37˚C. The plates were then for 48 hours at 37˚C and then examined for colony
=1 examined for surface colony growth and stained growth both on the agar surface and lower down
p = frequency of dominant allele with iodine solution to determine the extent of within the oxygen-poor agar layer.
q = frequency of recessive allele starch digestion. Table 2
Table 1 Surface Colony Growth Deep-Agar Colony Growth
p = frequency of dominant homozygotes
2
Once incubated, bacteria will grow if nutrients they can metabolize are available. Keep this in mind as you interpret the procedure and results.
Experiment 1 and Table 1: What are the important aspects? Two strains (1 and Experiment 2 and Table 2: Note the significant differences between the two
2) undergo identical incubation on 3 plates with different starch agars. Look at Table experiments. This time, the strains were separately distributed within the agar
1, one strain at a time. The researcher observes growth and starch digestion. Strain 1 instead of jointly streaked on top of multiple agars. The researcher observes
grows on all plates, but doesn’t digest the starch: it must be using another nutrient to growth on top and within, the assumption being that the top is oxygen-rich and
grow. We don’t know that Strain 1 can’t digest starch—we just know that it’s not within is oxygen-poor. What does it mean that Strain 1 only grows in an oxygen-
digesting it in the first 48 hours. Strain 2 uses starch to grow on plates A and B, but rich environment? It is an obligate aerobe that requires oxygen for metabolism.
doesn’t digest starch or grow on plate C. Again, we don’t know that Strain 2 can’t What does it mean that Strain 2 can grow in oxygen-rich and oxygen-poor
digest the starch in medium C—we just know it’s not doing so in the first 48 hours. environments? It is a facultative anaerobe.
Regions of Example
Geometric Arrangement
of Electron Pairs around Shape Angle between KINETICS & EQUILIBRIUM
Electron Density Electron Pairs
the Central Atom
Experimental determination of rate law: The values of
k, x, and y in the rate law equation (rate = k[A]x[B]y) Eauncatalyzed
free energy
function of the initial concentrations of the reactants, A Eacatalyzed
and B.
catalyzed
Efficiency of Reactions
reaction coordinate
Law of Mass
free energy
Eaforward
H2 + Cl2 Eareverse
Action aA + bB -~-- cC +
ΔG
dD - c
[C]
Kc = d
Complex Ion (Coordination Compound) [D]
2 HCl a b
A Lewis acid–base adduct with a cation [A] [B]
reaction coordinate Kc is the equilibrium constant (c stands for
bonded to at least one electron pair donor concentration).
(including
water). Donor molecules are called ligands and use COMPOUNDS & STOICHIOMETRY
coordinate covalent bonds. The central cation can
Properties of the Equilibrium Constant
be bonded to the same ligand multiple times in a A mole is the amount of a substance that contains Pure solids and liquids don’t appear in expressions.
process called chelation. the same number of particles that are found in a
12.000 g sample of carbon-12. Keq is characteristic of a given system at a given
temperature.
The molecular or formula weight is measured in amu
If Keq >> 1, an equilibrium mixture of reactants
per molecule (or formula unit). The molar mass is
measured in grams per mole. and products will contain very little of the reactants
compared to the products.
Combustion reactions: A fuel, such as a
hydrocarbon, is reacted with an oxidant, such as If Keq << 1, an equilibrium mixture of reactants
oxygen, to produce an oxide and water. and products will contain very little of the products
compared to the reactants.
CH4 (g) + 2 O2 (g) → CO2 (g) + 2 H2O (g)
If Keq is close to 1, an equilibrium mixture of
Combination reactions: Two or more reactants products and reactants will contain approximately
form one product. equal amounts of the two.
S (s) + O2 (g) → SO2 (g) Le Châtelier’s principle is used to determine the
Intermolecular Forces direction in which a reaction at equilibrium will
1. Hydrogen bonding: The partial positive charge Decomposition reactions: A compound breaks down proceed when subjected to a stress, such as a
of the hydrogen atom interacts with the partial into two or more substances, usually as a result of change in concentration, pressure, volume, or
negative charge located on the electronegative heating or electrolysis. temperature. The key is to remember that a
atoms (F, O, N) of nearby molecules. 2 HgO (s) → 2 Hg (l) + O2 (g) system to which these kinds of stresses are applied
tends to change so as to relieve the applied stress.
Single-displacement reactions: An atom (or ion) of
δ– one compound is replaced by an atom of another In a nutshell:
δ+ δ+
element.
Zn (s) + CuSO4 (aq) → Cu (s) + ZnSO4 (aq)
δ+ δ– Double-displacement reactions: Also called
δ+ metathesis reactions; elements from two different
compounds displace each other to form two new
2. Dipole–dipole interactions: Polar molecules compounds.
orient themselves such that the positive
CaCl2 (aq) + 2 AgNO3 (aq) → Ca(NO3)2 (aq) + 2 AgCl
region of one molecule is close to the
negative region of another molecule. (s)
Net ionic equations: These types of equations
are written showing only the species that actually
δ+ H Cl δ– δ+ H Cl δ–
participate in the reaction. Consider the following THERMOCHEMISTRY
equation: The law of conservation of energy dictates that
Zn (s) + Cu2+ (aq) + SO2–4 (aq) → energy can be neither created nor destroyed, but that
δ+ H Cl δ– Cu (s) + Zn2+ (aq) + 2– (aq)
SO4 all thermal, chemical, potential, and kinetic energies
The spectator ion (SO2–) does not take part in the are interconvertible.
4
3. Dispersion forces: The bonding electrons in overall reaction, but simply remains in solution
covalent bonds may appear to be equally throughout. The net ionic equation would be: Systems:
shared between two atoms, but at any Isolated: no exchange of energy/matter with the
Zn (s) + Cu2+ (aq) → Cu (s) + Zn2+ (aq)
particular point in time they will be located environment. Bomb calorimetry creates a nearly
randomly throughout the orbital. This Neutralization reactions: These are a specific type isolated system.
permits unequal sharing of electrons, causing of double-displacement reactions that occur when
transient polarization and Closed: can exchange energy but not matter with the
an acid reacts with a base to produce a solution of environment
counterpolarization of the electron clouds of a salt (and, usually, water):
neighboring molecules, inducing the Open: can exchange both energy and matter
HCl (aq) + NaOH (aq) → NaCl (aq) + H2O (l) with the environment. Human beings are open
formation of more dipoles.
symmetrical asymmetrical
Factors affecting reaction rates: reactant systems because they can take in energy and
distribution
electron
distribution concentrations, temperature, medium, catalysts matter (eat), release matter into the
+ – Catalysts are unique substances that increase environment (respiration, urination, defecation),
δ δ
reaction rate without being consumed; they do and release energy into the
nucleus
this by lowering the activation energy. environment (heat transfer from the skin and mucous
membranes).
System processes: THE GAS PHASE
Isothermal: temperature of system remains constant
1 atm = 760 mmHg ≡ 760 torr = 101,325 Pa Deviations due to pressure: As the pressure of
Adiabatic: no heat exchange occurs a Do not confuse STP with standard conditions—the gas increases, the particles are pushed closer
Isobaric: pressure of system remains constant and
Isovolumetric (isochoric): volume remains constant two standards involve different temperatures and are closer together. At moderately high pressure, a gas’s
used for different purposes. STP (0˚C or 273 K, 1 atm) volume is less than would be predicted by the
Heat: the transfer of thermal energy from one object ideal is generally used for gas law calculations; standard gas law due to intermolecular attraction.
to another. conditions (25˚C or 298 K, 1 atm, 1 M concentrations) Deviations due to temperature: As the temperature
is used when measuring standard enthalpy, entropy, of a gas decreases, the average velocity of the
Endothermic: reactions that absorb heat energy
Gibbs free energy, and electromotive force. gas molecules decreases and the attractive
Exothermic: reactions that release heat energy intermolecular forces become increasingly
Boyle’s Law significant. As the temperature of a gas is reduced,
endothermic exothermic intermolecular attraction (a) causes the gas to
PV = k or P1 V1 = P2 V2 have a smaller volume than would be predicted. At
heat extremely low temperatures, the volume of the gas
heat Charles’s Law particles themselves (b) causes the gas to have a
V = k orV1 =
V2
larger volume than would be predicted.
T T1 T2
Van der Waals equation of state: accounts for the
heat Gay-Lussac’s Law deviations from ideality that occur when a gas does
P P1 P2
= k or = not closely follow the ideal gas law
T T1 T2 2
heat (P + n a )(V – nb) = nRT
heat Avogadro’s Principle V2
n n1 n2
Constant-volume and constant-pressure calorimetry:
= k or =
used to indicate conditions under which the heat V V1 V2 1 mole of gas at STP = 22.4 L
changes are measured Combined Gas Law Dalton’s law of partial pressures: states that the
q = mc∆T, where q is the heat absorbed or Integrates Boyle’s Law, Charles’s Law, and Gay- total pressure of a gaseous mixture is equal to
released in a given process, m is the mass, c is the Lussac’s Law the sum of the partial pressures of the
specific heat, and ∆T is the change in temperature individual
P1V1 P2V2 components
States and state functions: are described by the =T
macroscopic properties of the system. These T1 2
properties’ magnitudes depend only on the PT = PA + PB + PC +…
Ideal Gas Law
initial and final states of the system, and not on PA = PTXA
the path of the change. Common state functions PV = nRT
include pressure, density, temperature, volume, nA (moles of A)
enthalpy, internal energy, free energy, and
Real Gases where XA =
nT (total moles)
entropy.
Enthalpy (H): is used to express heat changes at Kinetic molecular theory of gases: an explanation of
constant pressure gaseous molecular behavior based on the motion
of individual molecules
Standard heat of formation (∆H°f ): the enthalpy
Average molecular speeds
change that would occur if one mole of a compound
1 3
was formed directly from its elements in their K= mv2 = kBT
standard states 2 2
Standard heat of reaction (∆H°rxn): the hypothetical Decreasing the volume of a sample of gas makes it Root-mean-square speed
behave less ideally because the individual gas particles
enthalpy change that would occur if the reaction
were carried out under standard conditions
are in closer proximity in a smaller volume. (They are urms = (3RT
∆H° = (sum of ∆H° of products) –
rxn f
PHASES & PHASE CHANGES
(sum of ∆H° of reactants) Entropy (S): the measure of the distribution of energy
f (“randomness”) throughout a system
Hess’s law: states that enthalpies of reactions are ∆Suniverse = ∆Ssystem + ∆Ssurroundings
additive
Gibbs free energy (G): combines the two factors
The reverse of any reaction has an enthalpy of the that affect the spontaneity of a reaction—changes in
same magnitude as that of the forward reaction, but enthalpy, ∆H, and changes in entropy, ∆S
pressure
energy
equilibrium; thus, ∆G = 0 and ∆H = T∆S. gas
temperature
Colligative properties: These are physical properties
derived solely from the number of particles present,
not the nature of those particles. These properties
Bond enthalpy: The standard heat of reaction are usually associated with dilute solutions. Molality
can be calculated using the values of bond (m) must be used, in addition to the van ’t Hoff factor
Reaction quotient (Q): Once a reaction commences,
dissociation energies of particular bonds (i) for ionic compounds.
the standard state conditions no longer hold. For the
(given in a table). reaction: Freezing point depression
∆ H° n
rx
= ∑∆ H bonds broken
−∑∆ Hbondsformed
aA + bB ~ - -cC + dD ∆Tf = iK fm
c d
[C] [D] Boiling point elevation
Q= a b
[A] [B] ∆Tb = iKbm
Osmotic pressure ACIDS AND BASES REDOX REACTIONS & ELECTROCHEMISTRY
∏ = MRT
Arrhenius definition: An acid is a species that Oxidation: loss of electrons
produces excess H+ (protons) in an aqueous
Vapor pressure lowering (Raoult’s law) solution, and a base is a species that produces Reduction: gain of electrons
PA = XAPA˚ ; PB = XBPB˚ excess OH– (hydroxide ions). Oxidizing agent: causes another atom to undergo
Solutions that obey Raoult’s Law are called ideal Brønsted–Lowry definition: An acid is a species oxidation, and is itself reduced
solutions. that donates protons, while a base is a species
Reducing agent: causes another atom to be reduced,
125 that accepts protons.
heating of water vapo r
and is itself oxidized
Lewis definition: An acid is an electron pair acceptor,
100
and a base is an electron pair donor.
heat used to vaporize water to Galvanic Cells
water vapor
temperature (˚C)
75
Both diffusion and effusion have the same formula: Hydrolysis: This is the reverse reaction, where the salt
ions react with water to give back the acid and base. Electrolytic Cells
r1 m
1
2
= r Amphoteric species: is one that can act
m 2
1 either as an acid or a base, depending on its
2
chemical environment e
SOLUTIONS
Titration and Buffers
1. All salts containing alkali metal (Group 1) Titration is e
or ammonium (NH+) cations are water- a procedure
soluble. 4 used to
2. All salts containing the nitrate (NO–) or acetate determine the
3
(CH3COO–) anions are water-soluble. molarity of an
3. All chlorides, bromides, and iodides are water- acid or base
soluble, with the exception of Ag+, Pb2+, and by reacting a
Hg2+. known volume
4. All salts of the sulfate ion (SO42–) are water- of a solution
A redox reaction occurring in an electrolytic cell
soluble, with the exception of a2+, Sr2+, of unknown
Ba2+, concentration has a positive ∆G and is therefore
C strong acid and strong base
and Pb2+. nonspontaneous. In electrolysis, electrical energy is
with a known required to induce a reaction. The oxidation and
5. All metal oxides are insoluble, with the volume of
exception of the alkali metals and CaO, SrO, reduction half-reactions are usually placed in one
a solution container.
BaO, all of which hydrolyze to form solutions of known
of the corresponding metal hydroxides. concentration. Reduction potential of each species is defined
6. All hydroxides are insoluble, with the exception as the tendency of a species to acquire electrons
The half-
of the alkali metals and Ca2+, Sr2+, and Ba2+. equivalence and be reduced. Standard reduction potential, E
7. All carbonates (CO 2– 3–),
3 ), phosphates (PO 4 point defines ˚, is measured under standard conditions: 25˚C,
2–
sulfides (S ), 2–
ulfites (SO ) are pH = pKa 1 M concentration for each ion in the reaction, a
soluble,
and s in partial pressure of 1 atm for each gas and metals
3
with the exception of the alkali metals and BA SIC in their pure state.
ammonium. weak acid and strong base Standard reduction potentials are used to calculate
Henderson–Hasselbalch equation: the standard electromotive force (emf or Ec˚ell) of a
Units of Concentration 3
reaction, the difference in potential between two
is used to estimate the pH of a 3
Percent composition by mass: solution in the buffer region where the half-cells.
Mass of solute concentrations of the species and its
emf = Er˚ed, cathode – Er˚ed, anode
Mass of solution × 100% conjugate are present in approximately
equal concentrations 2 3
# of mol of compound Gibbs free energy, ∆G, is the thermodynamic
Mole fraction: total # of moles in system [conjugate base] 4
criterion for determining the spontaneity of a
pH = pKa + log [weak acid]
4
reaction.
# of mol of solute
Molarity: liter of solution ∆G = –nFEcell
[conjugate acid]
pOH = pKb + log [weak base] A C IDIC
Molality: # of mol of solute
kg of solvent
PLAN ORGANIC CHEMISTRY
| MCAT QUICKSHEETS I
NOMENCLATURE ISOMERS
1. Find the longest carbon chain containing the
principal functional group (highest-priority
groups are generally more oxidized).
2. Number the carbon chain so that the principal
functional group gets lowest possible number.
3. Proceed to number the chain so that the lowest Physical properties are characteristics of processes that
set of numbers is obtained for the substituents. don't change the composition of matter, such as melting
Name the substituents and assign each a number. point, boiling point, solubility, odor color, and density.
5. Complete the name by listing substituents in Chemical properties have to do with the reactivity of
alphabetical order; place commas between the molecule with other molecules.
numbers and dashes beMeen numbers and words.
cn, Stereoisomers
nc— Conformational isomers
CH, c«, cu, differ by rotation around a single (a) bond
• Staggered conformgtions have groups 60° apart,
Ebutyl neopentyl isopropyl " " " " as seen in a Newman projection. anłfi ——
CH, largest groups are 180° apart; gauche -- 60°
CHy-CHy- H— • apan.
Eclipsed confbmations have groups directly in
see-butyl isobupl front of each other. TotaEy eclipsed = largest groups
as directly in front of each other; strain is maximized.
Functionąl
Group Prefix SuTx
Bond order single double triple
Carboxylic acid car6axy— aie acid Comes from:
aIkanoęIox/- • Angte strain: stretch or compress angles from
Anhydrides onhydride 2 zr
carbon/I— normal size
Esters o//‹oxy’cardpnyl— —oare Hybridlzation sp3 sp' sp • Torsional strain: from eclipsing conformations
Amides carbomoyl— —amide • Nonbonded strain: from interactions with
oxo —a( Angles t09.5° 120° t80°
Aldehydes substituents on nonadjacent carbons. In
Ketones oxo— or keto— —one Example C—C C=C C-C cyclohexane, the largest substituent usually takes
Alcohols hydro›‹y— —ol equatorial position to reduce nonbonded strain
ALKANES
• Electronegativity: Nucleophilicity decreases
as electronegativity increases because these
atoms are less likely to share electron density.
Configurationa!Isomers
• Steric hindrance: Bulkier molecules are less
nucleophilic. Can only be interchanged by breaking and reforming
• Solvent: Protic solvents can inhibit bonds
Combustion nucleophilicity by protonating the nucleophile • Enantiomers: nonsuperimposable mirror
CąHg + 5 02 —+ 3 C02 + 4 H20 + or hydrogen bonding. images; have opposite stereochemistry at every
heat sx1 chiral carbon. Same chemical and physical
s,y2 In aprotic solvents, nucleophilicity parallels basicity:
properties except for rotation of plane-polarized
2 steps 1 step F— › Cl— › Be › I— light and reactions in a chiral environment
Favored in polar protic Favored in polar In protic solvents, good bases pick up protons and
solvents aprotic solvents are worse nucleophiles:
2‘ methy 3” I— › B › CI— › F—
rate k[RL, raee* k[Nut2RL] Electrophiłes
Optically active and Racemic mixtures and meso compounds are optimally
Rącernic products Electrophile = “electron-loving”; tend to have inactive.
inverted products a positive charge or positively polarized atom
Strong nucleophile not Favored with strong that accepts an electron pair from a nucleophile. • Diastereomers: non-mirror-image stereoisomers.
required nucleophile Electrophilicity is increased by increasing the positive Differ at some, but not all, chiral centers. They
charge. have different chemical and physical properties.
• Cis-trans: subtype of diastereomers in which
Most common electrophiles: groups differ in position about an immovable
• Carbonyl carbon bond (such as a double bond or in a cycloalkane).
• Substrate carbon in an alkane
• Carbocations Abso!ute Configuration
An alkene is (2’) if the highest-priority substituents
Leaving Groups are on the same side of the double bond, and (£) if
Leaving groups = molecular fragments that retain on opposite sides.
Nuc!eophi!es the electrons after heterotysis (breaking a bond, A stereocenter's configuration is determined by
with both electrons being given to one of the putting the lowest-priority group in the back and
Nucleophile = “nucleus-loving”; tend to have two products). The best leaving groups will be drawing a circle from group 1 to 2 to 3 in
lone pairs or x bonds that can form new bonds able to stabilize the extra electrons. descending priority. If this circle is clockwise, the
to electrophiles. Nucleophilicity is increased by
Most common leaving groups: stereocenter is (/t); if it is counterclockwise, the
increasing electron density.
stereocenter is (S).
Nucleophilicity is determined by four major factors: • Weak bases
• Large groups with resonance
• Charge: Nucleophilicity increases with increasing
electron density (more negative charge). • Large groups with electron-withdrawing atoms
—+—+—++
Oxidizing Agents
H2SO4
Are the other reagents acidic or basic? Are they Good oxidizing agents have a high affinity for p-benzenediol 1,4-benzoquinone
(hydroquinone)
specific to a particular reaction? Are they good electrons (such
oxidation statesas(like O3,7+and
O2, Mn high4—,
Cl2) or unusuallyMnO
in permanganate,
nucleophiles or a specific solvent? Are they and Cr6+ in chromate, CrO42 These molecules can be further oxidized to form a
good oxidizing or reducing agents? —). class of molecules called hydroxyquinones.
Reducing Agents Many hydroxyquinones have biological activity.
Step 4: Identify the Most Reactive Functional Group(s) Good reducing agents include sodium, magnesium,
O
OH
More oxidized carbons tend to be more aluminum, and zinc, which have low electronegativities
reactive to both nucleophile–electrophile and ionization energies. Metal hydrides are also
reactions and good reducing agents, like NaH, CaH2, LiAlH4, and O
oxidation–reduction reactions. Note the presence of NaBH4, because they contain the H– ion.
protecting groups that exist to prevent a particular Ubiquinones
functional group from reacting. Ubiquinone is also called coenzyme Q and is a vital
electron carrier associated with Complexes I, II,
Step 5: Identify the First Step of the Reaction and III of the electron transport chain.
• If the reaction involves an acid or a Ubiquinone can be reduced to ubiquinol, which
base: protonation or deprotonation can later be reoxidized to ubiquinone. This is
• If the reaction involves a nucleophile: sometimes called the Q cycle.
nucleophile attacks electrophile, forming a bond
• If the reaction involves an oxidizing or ALDEHYDES
reducing agent: most oxidized
The dipole moment of aldehydes causes an
functional group is oxidized or reduced,
elevation of boiling point, but not as high as
accordingly
Oxidation alcohols because there is no hydrogen bonding.
Step 6: Consider Stereoselectivity • PCC takes a primary alcohol to an aldehyde.
PCC
Synthesis
If there is more than one product, the major product OH O
• Oxidation of primary alcohols
will generally be determined by differences in strain
or stability between the two molecules. Products • Jones’s reagent, KMnO4, and alkali • Ozonolysis of alkenes
with conjugation (alternating single and multiple dichromate salts will convert secondary
Reactions
bonds) are significantly more stable than those alcohols to ketones and primary alcohols to
carboxylic
OHacids. O Reactions of enols (Michael additions)
ALCOHOLS Na2Cr2O7
H2SO4 O O
Base
O O
+ H:Base
Synthesis Reduction R R R
— R
R R
O OH
• Addition of water to double bonds
Nucleophilic addition to a
• S N1 and SN 2 LiAlH4
carbonyl O — OH
or O
reactions of carboxylic acids, aldehydes,
+
H
• Reduction NaBH4
H H
H
ketones, and esters Nu Nu Nu
OH + HBr
OH
2 +
Br Alcohols can be used as protecting groups R
C
CH3 R
C
CH2 R
C
CH2
C
R R
C
C
C
R
H
for carbonyls, as reaction with a dialcohol enol
H
aldol addition product aldol condensation
product
Br OH
forms an unreactive acetal. After other
+ Br + H2O
reactions, the
2
Decarboxylation
protectingO group can
O
beO removed
O
with aqueous
O
O acid. O
HO OH H2O C
cat. H cat. H
LiAIH4 O
OH O
NaI
+ O S O + —SO
3 O O O O OH OH
I
LiAIH4 OH
ClSO 2
tosyl chloride
OH
+++
O +—Nanonpolar tail
+
polar head
Intramolecular formation of a cyclic anhydride
Nucleophilic acyl substitution O O
Reduction to an
Ester formation OH O + H2O
amine
OH
LiAlH4
O
O NH2 NH2
ortho-phthalic acid phthalic anhydride
Esters
Transesterification
• Reduction to alcohols
NITROGEN-CONTAINING COMPOUNDS
Hydrolysis
OH OH
+
OH
+
O
O
H2O O OH
H + H H
O
NH2 NH2
Saponification
−
CN R NH+ −H2O
2 O O
R R
OHN
2
RC O O+– Na
RC
+
N NH
+ OH
2 O O HO
H2N +
H H2N H2O H 2N
NaOH O– Na + HO
RC O RC
CYCLIC CARBOXYLIC ACID DERIVATIVES R R R
NH
O O HO
proton O– Na
Lactams transfer RC O RC
PHOSPHORUS-CONTAINING COMPOUNDS
+ NH
nitrogen: β-lactams contain a bond between the β- R
NH
3
R
NH
2
R
2
+
O inorganic phosphate includes both hydrogen
phosphate (HPO2–) and dihydrogen phosphate
H2N −H H2N
OH OH
O (H PO –
4 ).
R R
N N O N O N O 2 4
H H H H • Pyrophosphate (PPi ) is P2O74–, which is released
β-lactam γ-lactam δ-lactam ε-lactam Gabriel (Malonic-Ester) Synthesis during the formation of phosphodiester bonds
Reagents: potassium phthalimide, diethyl in DNA. Pyrophosphate is unstable in
Lactones bromomalonate aqueous solution, and is hydrolyzed to
O O O
form two molecules of inorganic
Cyclic esters are called lactones. These are CO2C2H5 CO2C2H5 CO2C2H5
phosphate.
− + base
N K + Br C H SN 2 N C H N C −
named not only based on the carbon bound to the CO C H
2 2 5
CO C H
2 2 5
CO C H
2 2 5
O O 4–
oxygen, but also the length of the carbon chain
O O
potassium diethyl
phthalimide bromomalonate
itself. P P
O − R–Br
O O
CO2H
H3 O , ∆
+ O CO2
−
CO2C2H5
SN2
O O O
O O
+
H3N C R
−CO 2 + H2N C R
NaOH
N C R O O
O H 2O, ∆
O H O CO2 − CO2C2H5
O O
–
O • Nucleotides with phosphate groups, such
O
O ATP, GTP, and those in DNA, are referred to
PURIFICATION METHODS SPECTROSCOPY
Extraction separates dissolved substances Distillation separates liquids based on boiling Infrared spectroscopy measures molecular vibrations
based on differential solubility in aqueous vs. point, which depends on intermolecular forces. of characteristic functional groups.
organic solvents. Types are simple, fractional, and vacuum. Functional Group Wavenumber (cm–1) Vibration
ArOH 4–12
to vacuum trap –COOH 10.5–12
glass projection to
–NH2 1–5
hold up packing
Ha Hb
clean filter flask deshielding b Cl C O C Hb
shielding Cl Hb
TMS
filtrate
a
Linear Motion • When solving for time, Power: the rate at which work is performed; it is
v = v, + af given by: P —— (SI unit: watt =S) Conservation of Energy
?at2 is initially launched and When there are no nonconservative forces (such as
Mechanical Energy friction) acting on a system, the total
V+2' ’j + 2ax ground.
Energy is a scalar quantity (SI unit: joule). mechanical energy remains constant: AT = AT
(v,+v) • To find max height, + AT = 0
2 Kinetic energy: the energy associated with moving
objects. It is given by:
v,+v 0 at the highest point of y_y2
2 Thermal Expansion
Linear expansion: the increase in length by most
Projectile Motion solids when heated
Mnemonic: when temperature increases, the length
v=O Newton's thirdl w:If body A exerts a'force on body of a solid increases “a Lot"(n£A/)
B, then B will exert a force back onto A that is
equal in magnitude, but opposite in direction. This ML —— UT
h can be expressed as Fg = —F,. Volume expansion: the increase in volume of fluids
Newton's law of gravitation: All forms of matter when heated
experience an attractive force to other forms of
matter in the universe. The magnitude of the force is
• Vertical component of velocity = v sin 8 Gm ’z Heat Transfer
represented by: F ——
• Horizontal component of velocity = v cos fi r’ Conduction: the direct transfer of energy via
Frictional forces • Mass (m): a scalar quantity that measures a molecular collisions
body's inertia Convection: the transfer of heat by the physical
Static friction (/s): is the force that must be
overcome to set an object in motion. It has the • Weight (F ): a vector quantity that measures motion of a fluid
formula: 0 < /, < ps/\/ a body's gravitational attraction to the earth
Radiation: the transfer of energy by electromagnetic
(Fq = mg)
Kinetic friction (/y): opposes the motion of objects waves
moving relative to each other. It has the formula: Uniform circular motion: •
Specific Heat
F,
g = mc&T (mnemonic: looks like MCAT)
F ——
/7IV • Can only be used to find Q when the object
r does not change phase
Equilibrium • Q › 0 means heat is gained; Q ‹ 0 means heat
is lost
First condition of equilibrium: An object is in
translational equilibrium when the sum of forces [Common units: joules, calories, or Calories (kcal)]
Newton's first law (law of inertia): A body in a state pushing it one direction is counterbalanced by the Heat of transformation: the quantity of heat required
of motion or at rest will remain in that state unless sum of forces acting in the opposite direction. It to change the phase of 1 g of a substance.
acted upon by a net force. can be expressed as OF = 0. Q = ml (p hase changes are isothermal processes)
NS
Newton's second law: When a net force is applied to First law of thermodynamics: AL/ = Q — W
a body of mass m, the body will be accelerated in the
same direction as the force applied to the mass. This Process First Law Becomes
is expressed by the formula F = ma [SI unit: Adiabatic (g = 0) bU —— —W
newton Constant \oIume (W = 0) gg q
kg m
(N) = ]. Isothermal (AL/ = 0) 0 —— w
• Fg pytj › F-¿ pg: QDFSOh
dCC9leFdt9S downward Second law of thermodynamics: In any
• Fy = F¿ y' terminal velocity thermodynamic process that moves from one state
is reached (person travels at
of equilibrium to another, the entropy of the system
Problem-Solving Guide and environment together will either increase or
• Resolve the forces into x- and y-components. remain unchanged.
• OF = 0 must be true for equilibrium;
therefore, SF, = 0 and SF = 0.
HYDROSTATICS & FLUID DYNAMICS ELECTROSTATICS CIRCUITS
m kg
Density (ρ) = [SI units: ] Coulomb’s Law Current: the flow of electric charge. Current is given
V ρ 3 by:
m kg Q C
Specific gravity = subtance
[no units]; ρ = 103 I= [SI units: ampère (A) = ]
∆t s
ρwater water 3
m +q1 –q2
F F (The direction of current is the direction positive
Weight = ρgV r charge would flow, or from high to low potential.)
Pressure: a scalar quantity defined as force per unit kq1q2
area: P =
F
[SI units: pascal =
N
]
F= 2 [SI units: newtons] Ohm’s Law and Resistance
A m
2 r
V = IR (can be applied to entire circuit or individual
• For static fluids of uniform density in a sealed Electric Field
vessel, pressure: P = ρgz resistors)
field lines ρ
• Absolute pressure in a fluid due to gravity Resistance: opposition to the flow of charge. R = L
somewhere below the surface is given by (Resistance increases with increasing temperaturesA
the equation P = Po + ρgz with most
+ –
• Gauge pressure: Pg = P – Patm conductors.) [SI Units:
Continuity equation: A1v1 = A2v2 ohm (Ω)]
1 Fe Q N V
Bernoulli’s equation: P + ρv 02 + ρgh = constant
2 E= = 2 [SI units: or ] Circuit Laws
q r C M
• A positive point charge will move in the same Kirchhoff’s laws:
Archimedes’ Principle
direction as the electric field vector; a negative 1. At any junction within a circuit, the sum of
Fbuoy = ρfluid gVsubmerged charge will move in the opposite direction. current flowing into that point must equal the
sum of current leaving.
N Electrical Potential Energy (U)
4
5
2. The sum of voltage sources equals the sum of
The electrical potential energy of a charge q at a point
3
1 7
Electric Dipoles b
0
3Ω Req = R1 + R2 + R3 + …
c VT = V1 + V2 + V3 + ...
5V 5Ω
• p is the dipole IT = I1 = I2 = I3 = …
E d
moment (p = qd). 7Ω
• The dipole feels no net Fe
translational force, but
experiences a torque
about the center
d Parallel Circuits
3 N displaced
causing it to rotate so Ip
that Fe=qE
1 1 1 1
the dipole moment aligns I1 I2 I3 In Req = R + R +R + ...
1 2 3
with the electric field.
• The buoyant force is equal to the weight of the Rp R1 R2 R3 Rn VT = V1 = V2 = V3 = ...
IT = I1 + I2 + I3 + ...
displaced fluid.
If the weight of the fluid displaced is less than Electrical Potential Ip
the object’s weight, the object will sink. The amount of work required to move a positive test
If the weight of the fluid displaced is greater charge q from infinity to a particular point divided by
U J
Power Dissipated by Resistors
than or equal to the object’s weight, then it the test charge: V = [SI units: volt = ]
2
V
q C
P = IV = = I2 R
will float. R
A1 A2
d2 Energy Stored by Capacitors 2
d1 1 1 2 1 Q
+V U= QV = CV =
W kQ J 2 2 2 C
F2 Voltage (∆V) = = [SI units: volt = ]
q r C
C1
• When two oppositely charged parallel plates
are separated by a distance d, an electric field
is created, and a potential difference exists Capacitors in series:
C2
between the plates, given by: V = Ed add as reciprocals,
then take reciprocal Cs
of sum C3
1 1 1 1
C eq = C1 + C2 + C 3 + ...
d E
C4
F F
P= 1
= 2
and A d = A d
A1 A2 1 1 2 2
Estimation
Describing Waves Finding the resultant using the component method:
Refraction Converging
Measures oflenses
Central Tendency and Distribution
Scientific notation: A method of simplifying •c Resolve vectors into x- and y-components
m
n = (speed of light = 3 × 108 S • Mean: the average of the data points;
Longitudinal by
calculations wave
reducing numbers to a significand v
) • Sum all the vectors in the x-direction to get the impacted heavily by outliersf>0
between one and ten and the exponent power of Snell’sresultant for θthe=x-direction,
law: n1sin and donthe
n2 sin θ2. When
1 2 > n1 , • Median: the central value of a data set; not
ten: 0.0000037 = 3.7 × 10–6. Allows estimation by same toward
light bends for the the
y-components
normal; when n2 < n1, light affected by outliers
powers of ten, which is often all that is necessary on • The
bends awaymagnitude of the resultant R = Rx A2 +y
from the normal. • Mode: the most common data point(s);
the MCAT. R
not affected by outliers
Multiplication: If you round one number up, round Right-Hand Rule for Finding Direction • Range: the difference between the largest and
Transverse
the waveto compensate.
other down • smallest valuebeyond
in a set;
theimpacted heavily
the by
of Cross-Product Resultant For an object focal length,
Division: If you round one number up, round the n outliers
image formed is real and inverted.
Thenright-hand rule is used
other up to compensate. to find the direction of a • Standard deviation:
For an object insideathemeasure
focal of how spread
length, the
Roots and Logarithms vector that is the product of out values
image are isfrom
formed the upright
virtual, mean; affected by
and enlarged.
two other vectors. If C = A ×
• outliers
There is no image formed if an object is at the
B, then C is represented by
Wave x2
x formulas
x x2 x x2 x x2 focal point. 2
1 the palm while A is
ƒ= represented by the thumb
1 1 6 36 11
T 121 16 256
and B is represented by the Diverging lenses
2 4 7 49 v = 12
ƒλ 144 17 289 Diffraction fingers.
(v ± v D )
Q
f ′ = f(v ∓ vS )
distribute healthcare resources fairly 900
Observer and detector moving apart:
Stationary source: vs = 0 Generalizability 25
– sign in numerator
Stationary detector: vD = 0 Statistical significance and causality do not make
800
• + sign in denominator 12.5 true speed
6.25
something generalizable or a good intervention. 3.125
1.5625
1 2 3 4 5 6 7
Clinical significance and the target population must 0
700
number of half-lives
also be considered.