Question 1 [Chemical
Bonding > Hybridisation and covalent bonding]
(a) Complete the diagrams to
show the energies of the electrons in a carbon atom, a C+ ion and a C– ion.
Reference: Past Exam Paper – Chemistry (9701) March 2016 Paper 42 Q1
Solution:
a)
C (6 electrons): 1s2 2s2
2p2 [2/3
subshells filled with 1 electron each]
C+ (5 electrons): 1s2 2s2
2p1 [1/3 subshells filled with 1 electron
each]
C- (7 electrons): 1s2 2s2
2p3 [all
3 subshells filled with one unpaired electron each]
b)
(i)Since
3 bonds are seen to originate from each carbon atom, hybridisation is sp2 (1+2=3)
(number
of bonds due to a type of hybridisation is equal to sum of powers of s and p
orbitals; eg: sp3 (1+3=4) therefore 4 bonds; tetrahedral shape. You
can also work backwards, CH4 = four bonds= 1+3= sp3 hybridisation)
(ii)
in an sp2 hybridisation, we have one unhybridised p orbital. Upon
reaction with excess hydrogen, this p orbital takes part in bonding with the H
atom. Per carbon, 1 unhybridised p orbital = 1 added H atom/ Carbon atom=>
final formula= c60H60
c)
[Substitution reactions in Arenes]
(i)
1: Cl2 and UV light (since substitution is made in side
chain and not on benzene ring)
2: AlCl3 and Cl2
(since substitution is made in benzene ring and not on side chain)
(ii)
every time we use UV light, the answer is FREE RADICAL SUBSTITUTION.
(iii)
Ideally, if carried out in excess, all hydrogen atoms on side chain are
substituted to give benzene-CCl3 {this
is the most appropriate answer}
Solutions provided by Kashish Varshney, India
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