Chapter 8: Q.60 (page 330)
Draw the major product formed when (R)-1-chloro-3-methylpentane is treated with each reagent: (a) ; (b) KCN; (c) DBU.
Short Answer
The major products formed from the given reagents are as follows:

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Chapter 8: Q.60 (page 330)
Draw the major product formed when (R)-1-chloro-3-methylpentane is treated with each reagent: (a) ; (b) KCN; (c) DBU.
The major products formed from the given reagents are as follows:

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Draw both theand E1 products of each reaction.

a.

b.
Rank the alkenes shown in the ball-and-stick models (A–C) in order of increasing stability.

Although there are nine stereoisomers of 1,2,3,4,5,6-hexachlorocyclohexane, one stereoisomer reacts 7000 times more slowly than any of the others in an E2 elimination. Draw the structure of this isomer and explain why this is so.
Draw a stepwise, detailed mechanism for each reaction.

a.

b.
Draw the products formed when each dihalide is treated with excess .

a.

b.

c.

d.
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