7.23: Solutions to Additional Exercises
- Page ID
- 122583
SN2
7-1
a)
b)
c)
d)
7-2
a)
b)
c) No reaction
d)
7-3
a)
b)
c)
7-4
First method:
Second method:
7-5 The second method is more efficient since the alkyl halide is not sterically hindered
7-6 H2O < NH2- < CH3CH2O-< CH3O-
SN1
7-7
7-8
a)
b)
c) No reaction
d)
7-9
a)
b)
c)
d)
7-10
a)
b)
c)
d)
SN2 vs SN1
7-11
a) SN2
b) SN2
c) SN1
d) SN1
7-12
a)
b)
c)
d)
7-13
a)
b)
c)
d)
e)
f)
g)
E2 vs E1
7-14
a)
b)
c)
7-15
a)
b)
c)
7-16
a)
b)
c)
d)
Substitution vs Elimination
7-17
a) Cl- ; strong nucleophile
b) NaH ; strong base
c) t-BuO- ; strong base
d) OH- ; strong nucleophile ; strong base
e) H2O ; weak nucleophile ; weak base
f) HS- ; strong nucleophile
g) MeOH ; weak nucleophile ; weak base
7-18
a) E2, SN1
b) SN2, E2
c) SN2
d) SN1, E1
e) E2, SN1
7-19
a)
b)
c)
d)
e)
7-20