(b) The Sn2 displacement by ammonia on bromocyclobutane or on chlorocyclobutane. (c) The SN2 displacement on (3R)-3-bromocyclohex-1-ene by sodium hydrosulfide (NaSH) or by sodium hydroxide.

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(b) The Sn2 displacement by ammonia on bromocyclobutane or on chlorocyclobutane.
(c) The SN2 displacement on (3R)-3-bromocyclohex-1-ene by sodium hydrosulfide (NaSH) or by
sodium hydroxide.
Transcribed Image Text:(b) The Sn2 displacement by ammonia on bromocyclobutane or on chlorocyclobutane. (c) The SN2 displacement on (3R)-3-bromocyclohex-1-ene by sodium hydrosulfide (NaSH) or by sodium hydroxide.
Which reaction in each of the following pairs would you expect to be faster?
(i)
Write both reactions using bond-line presentation and, using arrows providing a mechanistic
explanation of the course of the reaction, draw either a transition state or an intermediate
product of the reaction;
(ii) Shortly (one sentence) explain your reasoning why one of the two reactions will be faster.
Transcribed Image Text:Which reaction in each of the following pairs would you expect to be faster? (i) Write both reactions using bond-line presentation and, using arrows providing a mechanistic explanation of the course of the reaction, draw either a transition state or an intermediate product of the reaction; (ii) Shortly (one sentence) explain your reasoning why one of the two reactions will be faster.
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