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GENERAL CHEMISTRY I
MIDTERM
TUTOR CLASS
03. Atoms
1 Recommended
Textbook 3 How to Study General
Chemistry I
2 Our Folder
4 General Knowledge
I. Introduction to Chemistry
1. Recommended
Textbook
Chemistry -The Central Science, 13th
Edition:
https://drive.google.com/drive/folders/1XlszQ
lN2jWFX8xNfvZSCX-oAhANipKQK
3 Energy
6 Significant Figures
II. Matter & Measurements
1. Matter, Weight and Mass
Matter Matter is anything that has mass and occupies space (V and m)
Mass Measure of the quantity of matter in a sample of any material (same everywhere, universally)
Weight The force that is exerted on its mass by gravity (depends on P, varies universally)
P = mg
1. Mass is univerally the same, as long as you have a sample of matter
--> replace “mass” with “weight”
=> Misconception: 2. Weight in space is not “zero”, it’s so small, “almost zero” because gravitational force is:
Their is no “mass” in
space r super large <-> smaller weight
QUESTION:
IS PHOTON MATTER?
Yes
Non-matter: photon
II. Matter & Measurements
2. Physical States of Matters
State Transformation
Density
II. Matter & Measurements
2. Physical States of Matters
Characteristics Solid Liquid Gas Plasma
Ions, protons,
Composition Atoms/Molecules Atoms/Molecules Atoms/Molecules
electrons, neutrons
Fly chaotically in Fly chaotically in
Position of Particles Stuck in Lattice Slide on each other
all direction all direction
Movement of Particles Almost stationary Moderately fast Fast Very Fast
States are more the gas/liquid/solid thing, describing the qualitative behavior of some matter.
States This explains the sample at a given T and P.
H2O: solid (ice), liquid, gas (steam)
≠ CO2: solid (ice), liquid, gas (steam)
Phases describe a collection of matter (often a region) as opposed to that collection's state.
Phase This applies for a region uniform in chemical and physical.
H2O: 20 - 74,963 structures of solid (ice), liquid, gas (steam)
CO2: solid (dry ice), liquid (liquid 1), gas (carbonic gas), supercritical (liquid 2)
II. Matter & Measurements
2. Physical States of Matters
Phase Diagram of CO2 Phase Diagram of H2O
QUESTION:
WHERE DO YOU
NORMALLY FIND
PLASMA?
Volcanoes Electrical discharges in the sky above
the erupting volcano, not lava
In our daily life Too high energy, we don’t often see it
because our habitating environment
Lightning has a pretty low level of energy, or
“stable environment”.
Aurorae
All of them
II. Matter & Measurements
2. Physical States of Matters
Adding Salt (NaCl) to ice can cause
freezing-temperature depression
3
1 2 The interaction of NaCl(aq)
There’s always an + -
or Na and Cl , with H2O(l) is
NaCl can dissolve in H2O(l)
equilibrium between solid favorable => decrease
to form a solution of water
and liquid in the surface of freezing temperature of
and salt
ice: H2O (s) H2O (l) the solution => it melts
II. Matter & Measurements
2. Physical States of Matters
Basic Concepts
Pure Substance (in short: Substance): Matter that has distinct composition and
properties that does not vary from sample to sample (or Lab to lab)
Mixture: combination of > 2 substances, in which each substance retains its chemical
identity with NO chemical reaction occurs
Element: chemical comprising of only 1 type of atom
Compound: chemical comprising of > 2 types of atom
II. Matter & Measurements
2. Physical States of Matters
Homogenous: uniform structure or composition
throughout (D = const everywhere in the sample)
--> salt water (unsaturated or saturated with no crystal),
ethanol + water, pure water...
Heterogenous
Transformation Classification:
between Energy & Kinetic Energy (depending on the movement)
Potential Energy (depending on the storation)
Mass: E = mc 2 ΣE = E kinetic + E potential
c: speed of light (299 792 458 m/s) From High School:
E kinetic = mgh
E potential = _mv
1 2
2
II. Matter & Measurements
3. Energy
Laws of Thermodynamics
th If two bodies are each in thermal equilibrium with some third body, then they
0 are also in equilibrium with each other.
st Energy cannot be created or destroyed; it can only be converted from one form
1 to another.
nd Heat is transferred from one body to another body only if the two bodies are at
2 different temperatures.
rd The entropy of a system approaches a constant value as the temperature
3 approaches absolute zero.
th The dissipative component of evolution is in a direction of steepest entropy
4 ascent
II. Matter & Measurements
3. Energy
Thermodynamics in Reactions
st Energy cannot be created or destroyed; it can only be converted from one form
1 to another => If your process has the change in energy: ΔE => the process either
release or absorb E from the environment
P/S: lower
energy level
<=> more stable
IN COMMON
Energy is absorbed or released
QUESTION:
IS THE FOLLOWING
REACTION
EXOTHERMIC OR
ENDOTHERMIC?
>0
Exothermic
Endothermic
II. Matter & Measurements
4. SI Units
7 base units
II. Matter & Measurements
4. SI Units
Common Prefixes
II. Matter & Measurements
4. SI Units
Others
Derived SI Units: obtained by
multiplication or division
of one or more of the base
units
II. Matter & Measurements
4. SI Units
Transformation
between
Temperature
Units
II. Matter & Measurements
5. Uncertainty in Measurement
Types of Numbers
Exact numbers: those whose values are know exactly
--> a dozen of eggs = 12 eggs; number of B1 ssstudents..
The result has the same The result contains the same
number of decimal places number of significant figures
as the measurement with as the measurement with the
the fewest decimal places fewest significant figures
Combi nation
1 Origin of Atoms
2 Atomic Structure
III. Atoms
1. Origin of Atoms
Definition: building block of matter
Origin:
Eastern Philosophy Any mtter is made of Metal, Wood, Water, Fire, Earth
=> 2 Laws: kinds of atoms are constant. (water is H2O and never something else...)
General Concepts
1 mol = N A
atoms or molecules with the mass (in grams) = A (atomic mass
in amu) or M (molecular mass in amu) (see next slides)
1. Each element is composed of extremely small particles called atoms.
2. Element : all atoms of a given element are identical (except isotopes... see further) atoms
of different elements are different.
3. Atoms are unchanged in chemical reactions (The valence electrons change, not nucleus)
4. Compounds are formed when atoms of more than one element combine
5. A given compound always has the same relative number and kind of atoms
III. Atoms
2. Atomic Structure
Size of Atoms: 31 ~ 500pm
-10
Also use: 1Å = 10 m (Amstrong)
III. Atoms
2. Atomic Structure
Characteristics Protons (p) Neutrons (n) Electrons (e)
Surrounding the
Position In the nucleus In the nucleus nucleus, creating
electron shells
-19
Charge (e) +1 0 -1 1 e = 1.602 x 10 C
-27 -27
1 amu = 1.6605 x 10 kg
-31
Mass (kg) 1.6726 x 10 kg ≈ 1 amu 1.6749 x 10 kg ≈ 1 amu 9.1094 x 10 kg amu: atomic mass unit
= ___
1 m
Are held together by the strong atomic force. Point-like, dimentionless, 0 12
12
C
6
Other features Incase the nucleus is too big, the weak atomic dimention and are held in atoms
force allow radioactivity to occur by the electronic attractive force
with the nucleus
4 types of
radioactivity
QUESTION:
WHICH OF THE
FOLLOWING ARE
ISOTOPES?
c. 1.02 isn’t an integer and there are only two types of oxides
of Fe (FeO and Fe2O3) => there must be some Fe O in this
sample.
IV. Electronic Structures of Atoms
1 Concepts of Orbit &
Orbitals 4 Electron Configuration
2 Energy
5 Periodic
Characteristics
General Concepts Different electrons have different potential and kinetic energy
Each energy level correspond to a certain distance to the nucleus
Only valence electrons involves in chemical reactions
{electrons only have certain energy level, not all energy levels <=> only certain distances
=> from the nucleus, not all distances
discontinuous emmision spectrum
Classical
Certain Radii,
Physics is False Absorbance and
Circular Orbits Certain Definite “Allowed State”
in the Quantum Emision
Energies
1. the electron moves 3. An electron in a World 5. Energy is emitted or
around the proton in permitted orbit has a absorbed by the
circular orbits specific energy and is electron only as the
in an "allowed“ energy electron changes from
state one allowed energy
state to another
IV. Electronic Structures of Atoms
2. Energy
Only depends on n (principle quantum number) (see next slides)
< 0: since these Only applies for Hydrogen-like systems
are bound states:
Energy of an “allowed energy state” - Bohr
positive energy
must be given to extract
the
electron
You can also calculate ΔE
of a transition by using =>
ΔE = E 1- E2= _____ and then Wavelengths of the spectral lines of H
prove the following
formulae of 1/λ. Just
note that:
ΔE > 0 <=> absorbance
ΔE < 0 <=> emission
IV. Electronic Structures of Atoms
2. Energy
Only depends on n (principle quantum number) (see next slides)
Mathematically Proving:
IV. Electronic Structures of Atoms
2. Energy
Hydrogen-like systems: 1
electron + 1 nucleus
+ 2+ 3+ 4+ 5+ 6+
H, He, Li, Be, B, C, N,...
n: principle quantum number
∞
n --> <=> E --> 0 (atom lost its
+
electron) (H )
QUESTION: IN THE IDEAL CONDITIONS
(WITHOUT ENERGY LOSS), IF A COMPOUND
X ABSORBS THE PHOTON λ1 , IT WILL EMIT
PHOTONS WITH λ2WHERE:
IV. Electronic Structures of Atoms
2. Energy
Another Approach
IV. Electronic Structures of Atoms
2. Energy
Quantum Mechanics
1. A wave cannot be precisely localized ...
2. As electrons behave like waves they cannot be
precisely localized
3. More precisely we cannot know simultaneously their
speed and their position ( uncertainty principle)
4. There are described by wave functions which give
their probability of presence in some portion of
space and their energy
IV. Electronic Structures of Atoms
3. Quantum Numbers & Atomic Orbitals (AO)
General Concepts
Orbital: A region of space where the probability (P) of finding an electron: 100% > P > 90%. Each
orbital can only have 0, 1 or 2 electrons
Electrons have both particle and wave function => we can describe them by the Schrödinger’s
Equation:
3 first quantum numbers are solutions of the Schrödinger’s Equation, the last one is derived.
Each orbital is characterized by a set of 3 quantum numbers: n, l, m l
Each electron is characterized by a set of 3 quantum numbers: n, l, ml , ms
IV. Electronic Structures of Atoms
3. Quantum Numbers & Atomic Orbitals (AO)
Characteristics n l ml ms
Possible Values 1, 2, 3, 4, ... 0, 1, 2, ..., (n - 1) -l,... , 0,... , +l 1
+ ______
2
Mathematic Expression ∈ N* ∈ N* ∩ [0;(n-1)] ∈ N* ∩ [-l;+l)] { 1
∈ + _____
2 }
Principal quantum Azimuthal/Angular Magnetic quantum Spin quantum
Names
number Momentum quantum number number
number
natural plus or minus one
Values in Words positive integers integers from -l to
numbers/positive over two
+l
integers and zero
As n increase: From values of l, we have First or Second electron in
Bigger Orbital different types of orbitals the orbital. Electrons
The e spends more with different shapes: Describes the actually doesn’t spin, its
Meanings/Characteristics times further from the l = 0 (s) (sharp) orientation of the values are due to Pauli
nucleus <=> higher l = 1 (p) (principle) orbital in space Exclusion Principle: there
energy level l = 2 (d) (diffuse) aren’t two electrons with
less bound to the l = 3 (f) (fundamental) the same quantum state
nucleus For the same n, l increase <-> higher energy level
IV. Electronic Structures of Atoms
3. Quantum Numbers & Atomic Orbitals (AO)
Illustrations of values ml of p orbitals: Illustrations of d orbitals:
QUESTION: FOR THE SAME n , WHY DOES
HIGHER l MEANS HIGHER ENERGY LEVEL?
We have to look in terms of the whole system:
Lower l <=> more symetric and simple shape
of orbitals, and these orbitals (with
electrons inside) repels each other <=> in a
whole system, symetry means cancel out
forces
Lower l <=> less orbital with the same type
(considersing the possible values of m l) <=>
less repelling forces
- l = 0 <=> only 1 AO (only 1 possible value of m l)
- l = 1 <=> 3 AOs (3 possible values of ml )
- l = 2 <=> 5 AOs (5 possible values of m l)
- l = 3 <=> 7 AOs (7 possible values of m l)
This can also explains an exception: 3d has
higher energy level than 4s. Anoter aspect
can be approached by penetration.
QUESTION: FOR THE SAME n , WHY DOES
HIGHER l MEANS HIGHER ENERGY LEVEL?
PENETRATION: WHEN ELECTRONS OF OUTER
SHELLS GETS CLOSER TO THE NUCLEUS
(PENETRATE INTO LOWER SHELLS).
The ability of penetration: s > p > d > f
Better penetration <=> lower energy level
IV. Electronic Structures of Atoms
3. Quantum Numbers & Atomic Orbitals (AO)
Summary:
All AOs with the same n = shell AOs same n and l <=> same energy level
All AOs with the same n and l = subshell
In shell number n there are n subshells
The total number of orbitals in a shell is n2
IV. Electronic Structures of Atoms
3. Quantum Numbers & Atomic Orbitals (AO)
Shape of Orbitals:
https://chem.libretexts.org/Courses/University_of_Arkansas_Little_Rock/Che
m_1402%3A_General_Chemistry_1_(Belford)/Text/6%3A_The_Structure_of_Ato
ms/6.6%3A_The_Shapes_of_Atomic_Orbitals
Nodal plane: yz xz xy
}
SHAPES & NODAL PLANES, NODES:
spherical (l = 0)
NO NODAL PLANE, NO NODE
} dumbell (l = 1)
1 NODAL PLANE, 1 NODE
xz and yz xy and yz
}
2 NODAL PLANES, 1 NODE
triple dumbell/others
When all AOs of a shell is filled (all are paired) => full shell
IV. Electronic Structures of Atoms
4. Electron Configuration
DEFINITION:
The way in which the electrons are distributed among the various orbitals of an
atom. The most stable electron configuration of an atom is the ground state = the
lowest possible energy state. Orbitals are “filled“ in order of increasing energy,
with no more than two electrons per orbital.
1. Electrons must be filled in orbitals subshells of lowest energy level (1s)
3. In a subshell, electrons must be filled to maximum spins (ms) (Hund’s Rule) (Write all possible electrons
with spins +1/2 before moving on to those of -1/2). Please mind the exception of Cu and Cr.
4. When drawing: each orbital is a square: and then write electrons in there. Spin +1/2 is an upward
arrow: and spins -1/2 is a downward arrow: .
not possible 5. When drawing, you should also draw the in accordance to
energy level (higher-energy AOs should be drawn higher) and
paired >< unpaired
same-energy-level AOs should be drawn as “stuck” together.
IV. Electronic Structures of Atoms
4. Electron Configuration
HOW TO WRITE?
1. Base on the Aufbau Principle to determine which AOs has lower
energy level Aufbau Principle:
start
2. For each subshell s, p, d, f, you must know how many AOs are
there (l = 1 <=> s <=> 1 AO
l = 2 <=> p <=> 3 AOs
l = 3 <=> d <=> 5 AOs
l = 4 <=> f <=> 7 AOs) and add electrons in those orbitals
(maximize spins (+1/2) before pairing (add -1/2 spins)
3. Denote them as following:
number of electrons in that subshell
n - principle quantum number + shorten name of AO (s, p, d or f from values of l)
Example:
QUESTION:
ELECTRON CONFIGURATION
HOW TO DO?
1. Remember and look at the Aufbau Principle to determine AOs
from lowest to highest: 1s 2s 2p 3s 3p 4s 4d ...
start
#Remember: The number of possible AOs in a subshell:
s - 1 AO p - 3 AOs d - 5 AOs f - 7 AOs
Here, you only have 14 electrons of Si, thus, you only have to
take subshells that provides around 7 AOs => you only need:
1s (1AO) + 2s (1 AO) + 2p (3 AOs) + 3s (1 AO) + 3p (3 AOs)
AO with same n = 3, l = 1 have the same E
=> 1s 2s 2p 3s 3p
}
level and are drawn as “stuck” together
=>
HOW TO DO?
E
3. Fill 14 electrons in those orbitals (next slide)
#Remember: - 1 AOs can hold a maximum of 2 e
- maximize spins as much as possible
- electrons are filled from low to high E level
After the total spin of the 2p subshell is maximized
=>
(3 x +1/2 = +3/2) (3 unpaired electrons in each AO 2p), we
can start filling electrons with spin -1/2.
E Now we have 14 - 2 - 2 - 4 = 4 electrons left.
E
=>
HOW TO DO?
E
3. Fill 14 electrons in those orbitals (next slide)
#Remember: - 1 AOs can hold a maximum of 2 e
- maximize spins as much as possible
- electrons are filled from low to high E level
After fullfilling the 2p subshell, we can move to the 3s
=>
subshell and fullfill it like any other s subshell.
Now we have 14 - 2 - 2 - 6 - 2 = 2 electrons left. We shall
E fill them in the 3p subshell in the same manner with the
2p subshell.E
=>
HOW TO DO?
E
4. Now we shall count the number of e in each subshell
and denote them as regulations.
}
}
}
}
}
electrons 2 2 6 2 2
1s2 2s2 2p6 3s2 3p2 => Choose A
P/S: Another tricky way: In B: the AO 3s (lower E) is not fullfilled <=> the AO 3p mustn’t be filled => B wrong
=> Choose A
IV. Electronic Structures of Atoms
4. Electron Configuration
10 2 6
≡
Ar - 18 e - [Ne]3s2 3p6 (10 + 8 e) => In the previous question of Si: 1s22s22p6 3s23p2 [Ne]3s2 3p2
Kr - 36 e - [Ar]3d 4s 4p (18 + 10 + 8 e)
10 2 6
Xe - 54 e - [Kr]4d 5s 5p (36 + 10 + 8 e)
14 10 2 6
Rn - 86 e - [Xe]4f 5d 6s 6s (54 + 14 + 10 + 8 e)
14 10 2 6
Og - 116 e - [Rn]5f 6d 7s 7p (86 + 16 + 10 + 8 e)
IV. Electronic Structures of Atoms
4. Electron Configuration
02 EXCEPTIONS
1 Effective Nuclear
Charge 3 Ionization Energy
CARBON SODIUM
V.
V. The
The Periodic
Periodic Table
Table
1.1. Effective
Effective Nuclear
Nuclear Charge
Charge
See Also:
In the periodic table. The effective nuclear charge
Penetration increases as we move across any row (period) of the
table.
Going down a column, the effective nuclear charge
(Previous experienced by valence electrons changes far less
than it does across a row.
Slides)
V. The Periodic Table
2. Size of Atoms and Ions
Size of Atoms
The closest distances separating the nuclei during
such collisions determine the apparent radii of the
argon atoms
V. The Periodic Table
2. Size of Atoms and Ions
Huger F <=>
Definition:
the minimum energy required to remove
an electron from the ground state of the
isolated gaseous atom or ion
This trend exists because with each successive removal, an electron is being pulled away
from an increasingly more positive ion, requiring increasingly more energy. The trend is clear
with some exceptions which can be explained by the inert-gas electron configuration or the
half-filled state
V. The Periodic Table
3. Ionization Energy
V. The Periodic Table
4. Electron Affinity
Definition: the energy change that occurs when an electron is
added to a gaseous atom
The End! Do you have Any Question?
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