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Summary - Alkenes, alkynes, cycloalkenes

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This document contains chapters 2 and 3 of an Organic Chemistry textbook. Chapter 2 focuses on alkanes and cycloalkanes, discussing their classification, structure, conformations, and reactions such as oxidation and halogenation. It includes detailed descriptions of their physical properties, hybridization, and isomerism. Chapter 3 covers alkenes and alkynes, elaborating on their nomenclature, properties, cis-trans isomerism, addition reactions, and mechanisms like electrophilic addition and hydroboration.

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Chapter 2 : Alkanes and cycloalkanes



G
n-bu

Three main classes of
1 .




hydrocarbons : But
-
Saturated Unsaturated, Aromatics
, see
-


non-polar (l-met
.
2 Alkanes are saturated hydrocarbons (InHan 2)+



109"




[
-


Hybridization : tetrahedral , sp3 ,
isob
-
unbranched alkanes are called n-alkanes (normal
let
-

Alkanes only differ by a
methylene group CH2 (1 , 1- d
-

Homologus : regular repetitive way-like of members in a compound
share Is
-
same
properties.
(2-m
-


Alkyl groups are alkanes -
1H atom (R-H) CnHan +1

CH3
-


neopentane : ↑

CH3 C C13
-
-




I

CH3

setroleum and natural the two important sources of
I gas are
-




alkanes , made of methane , then ethane then other higher alkanes
mostly .




-
If molecular weight is similar , alcohols have higher B .
P than alkan

-



C-C4 Gases 25-27 Liquids Co4 solids like wax


B p & weight (continuous chain)4
- .
molecular >
B Pb .




Bran
. Conformations/conformers
3 Stereo isomers

Newman projections :
H
4H °
rattached 60 rotation of the C-C bond
H- -H
toveat
↑ toton attached

it
H He H
H

staggered eclipsed of ethane


, 4 cycloalkanes nomenclature
%


cyclopropane is
necessarily planar (60 angle between carbon atoms to minimiz
·

Much less than the usual 109 5 .




angle of tetrahedral sp3 .




Formula of with Cuten
a
cycloalkane one
ring :

:
examples

4
CH3
Z




3-dimethylcyc
3
63-cyclohexyl heptane ↑
I
1
sa
#
5 ,


I longest carbon chain
/ Y
>
- substituent
CU3

-




Rotating alkanes (& cyclohexane) is easier than
rotating
-
In cyclobutane and cyclopropane , puckering allows the molecu

Cleast strain energy) .




H
chair conformation cyclohexane /

↳I
of



-
I

for methyl cyclohexane methyl , group on axial is less stable tha

( Because of diaxial interaction)


1-tetr-butyl-4-methylcyclohexane (d) most sta




A
(a) least st

(2) is more s

S Ha +
/
S d 7 c7b7a
in3 A cus e
in3 A
2




=
Ring flips :
(9) (b) (C) (d)
up -up
5 Cis-trans .
(geometrical) isomerism down dow

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Uploaded on
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Number of pages
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Written in
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Type
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