Chapter 8: Q.6 (page 303)
Which alkene in each pair is more stable?
a.
b.
c.
Short Answer
a. In the case of a., the stable structure is:
b. In the case of b., the stable structure is:
c. In the case of c., the stable structure is:
Chapter 8: Q.6 (page 303)
Which alkene in each pair is more stable?
a.
b.
c.
a. In the case of a., the stable structure is:
b. In the case of b., the stable structure is:
c. In the case of c., the stable structure is:
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Get started for freeDraw all constitutional isomers formed in each elimination reaction. Label the mechanism as E2 or E1.
a.
b.
c.
d.
e.
f.
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.
Pick the reactant or solvent in each part that gives the faster elimination reaction.
a. reaction of with 1-chloro-1-methylcyclohexane or 1-chloro-3-methylcyclohexane
b. reaction of with or
c. reaction of with in or DMSO
Rank the alkenes shown in the ball-and-stick models (A–C) in order of increasing stability.
Draw both theand E1 products of each reaction.
a.
b.
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