bromination
Br2/ ALbr3
electrophile
electron pair acceptor
which is major product secondary or tertiary
carbocation Intermidate is more stable in E (secondary than tertiary)
major formed from secondary carbonation
sterisomers
compounds with same structure formula but different arrangement In space
forming a pi bond
p orbitals overalp
amine and HCl
c- Nh3 + cl-
nitrogen electrop pair accepts a H +
why is the repeat polymer biodegradable
ester can be hydrolysed
explain the difference in solubitiyy of hexan 1 ol and hexane 1,6 diol
1,6 diol has 2 oh groups
forms more H bond with water
primary alcohol oxidised
carboncylix acid or aldehyde
2 (0. v. (0)
+h20 at end
test with na2co3
carboxylic acid
ph = 5
weak acid
so phenol
tollens reagents
tests for aldehyde
2,4 DNP
orange PPT
if carbonyl compound
homologous series
series of organic compounds with same functional group but with each successive member differing by CH2
hetrolytic fission
one bonded atom receives both electrons
breaking of covalent bond
explain the use of two deuterated compounds in NMR spectroscopy
D20 - used to identify OH peak and NH peak
CDcl3 - used as a solvent
strength of sigma bonds and pi bonds
sigma stronger
limitations of radical substitution
1- further substitution
2- mixture of products formed
resistance of chlorination with alkene and benzene
1-
ALKENE
electrons are localised
electron density is higher
more susceptible to electrophilic attack
BENZENE
electrons are delocalised
alkene + cl2
alkane cl2
sigma bonds
overlapping obitals between atoms
pi bonds
sideways overlapping p orbitals
why cant form sterisomers
c-c cannot rotate
2 groups on one carbon atom are the same
why boiling point increases with increase number of repeat units
more points of contact
stronger LF
more energy Required to break IMFS