Chapter 8: Q.20 (page 318)
Which mechanism, E1 or E2, will occur in each reaction?
a.
b.
c.
d.
Short Answer
The products with their mode of reaction are shown below:-
Chapter 8: Q.20 (page 318)
Which mechanism, E1 or E2, will occur in each reaction?
a.
b.
c.
d.
The products with their mode of reaction are shown below:-
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Get started for freeExplain why cis-1-chloro-2-methylcyclohexane undergoes E2 elimination much faster than its trans isomer.
Explain the selectivity observed in the following reactions.
Draw the products in each reaction.
a.
b.
c.
d.
For which reaction mechanisms—,E1, or E2—are each of the following statements true? A statement may be true for one or more mechanisms.
a. The mechanism involves carbocation intermediates.
b. The mechanism has two steps.
c. The reaction rate increases with better leaving groups.
d. The reaction rate increases when the solvent is changed from to localid="1648646954099" .
e. The reaction rate depends on the concentration of the alkyl halide only.
f. The mechanism is concerted.
g. The reaction of localid="1648646960420" with NaOH occurs by this mechanism.
h. Racemization at a stereogenic center occurs.
i. Tertiary (3°) alkyl halides react faster than 2° or 1° alkyl halides.
j. The reaction follows a second-order rate equation.
(a) Draw all products formed by treatment of each dibromide (A and B) with one equivalent of .(b) Label pairs of diastereomers and constitutional isomers.
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