Functional Groups

● In organic chemistry, a functional group is a specific group of atoms or bonds within a

compound that is responsible for the characteristic chemical reactions of that compound.

● Common examples are alcohols, amines, carboxylic acids, ketones, and ethers.
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Date-

ACID ANHYDRIDE

Ankyduide i klhe mmolecute tapable a_ Aouannig ads &oluio

HCd

Salttow ukstn ueactrl uwctw watue

foumulai (RcO) O_0u K-C0-0-co-R uulne Rou R
etal

Anugduiduy LLt take tlamaie anyduil au tybrel

Pucudtiu gg Auid

obtntu bthameia onluglesdz Àa liquial witw

Ploypnual
coloussmit stzongy umga (thonois
anid
stastmg_ut oikk
SmL du io the Liaasss augdusdlu

boilung Pamt Ghoos ankududt B:l i at l40C bitauu

fauly a big balas moleuls aid o had bott dghal dpal
attsactiomwaw d Waal! dipuon fos
ou it doun't lomm golegtn bozo mtami tisat BP
not a hglu as tat e a tawlomli ad at_bimilan sinp
 Date

Ouminal Þuapuutiu a aid_ahhyduus2

ubsttuon a
Pcid Anduide undugses a. uoopaig

comabantd to -0cOR erouk

Acuid. Atnkduilsu au stouely Aulualgudb the

LCH ) 0 + H0F 2Ha cooH
plmels to pualund etiu
Aid anludnds utoct utlw alcolsal!

co+CaH 0H CH,tooc H CH, CooH

L

uluidAe acio ambrgdu

LAMa uduud bu lttumw alumunum

amlekisde aluo mact tote pimaton ak atomot

aid
wit auomatu guaubous w the pn a
ert
aakapdrous alumihum chlouil

Symtin o Acid Antuduids

ChouA Dudd aa ig mbhatu o mnxly &0o°C B

MLastow & tom be Cpntdegd by tL Readion cnuloe

lazid uitl 2g-
+H20
HO
 alassMMte
Date
Page

o Acidl Anhgduides
Rcidu nhiugduidss laaue umol w w ugpmse oltmistsu-

phasmaceutcau, mdutbuial camuals, lois o

S23 o_esta by autylaten al alzoo
tiatdd n a4bliuw (acctyltalicylie ssel
uptlausaL_ kuáuar hy ducol deacetylato ag nwrplotist-
 Chea asnglane (2)

Niil s a uduekic cop<lynae) bmecd tfamu,

aCylowitile aua buthddeue combiuiuugbiiuq
i qoves ose me aodabl anslhds
Lowe allenga a e thal laex
R-CN OKT he-CEN paxt is t e lcuuctiae

Puysica pmoputies
Sohenat Coloaless salids q U9uids haiuguniqo
electoic sfzucime Siuilaa tn an alkud ody
Laiu Ifeaeuco is Hee tae euce
&ef Coe p a i t .
bCanlo uitogn on Spap ayloidis
ic Ceaues 4kh eot itt ooity LwitU

Rat oYeAlad t Faan P oid

T The R-CN bose angle( Caabbn &imlo

uPas gLape

aChaicad mpedies
D fn te'uitugaa beiug sp Luyhridlseds
aciic poDeadies
LLs oakic a

b)Paecu eectoucgati ye ifogeIA Cowle

itils to be rey Palal sausloculer
: fils fed fo aaie taialaea oilig
ofuks han wdeeulu _oitt Va Siuular
b

N
O ila aa i nmaiy
u l y unamwactued
wa by
acids L am wudiui

ortta pospLao u
elutoDsid Compo LAnd
ieac Dug
dengoea Maainus ro c O
eackios _

Peduetio ALKulatin

R- = NE+Hue

oke u _behaveA Siwilau to e

R CEN.
A

Nitila Canlovuyic acid