Question

5. For the following reaction: a) draw the substitution product. Br. но CH, b) Draw the full mechanism of the reaction above,
c) Draw the full mechanism of the reaction above, showing an Sn1 pathway. Include all relevant electrons and curved arrows sh
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Answer #1

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SN2 (Bimolecular Nucleophilic Substitution) Reaction :- This reaction is a single step reaction, in which transition state is formed which is highly unstable and form products. This reaction is a second order reaction.

SN1 (Unimolecular Nucleophilic Substitution) Reaction :- This reaction occurs at two steps. First step is the slowest step in which stable carbocation is formed and in the second step attack of weak nucleophile takes place on carbocation which is the fast step. This reaction is a first order reaction.

-ctz Bal . SN Mechanism ! -- Bs +- Bg slow CH3 391 · 9). Sn? Mechanism : choniemi Transit lon State Slow Stepi t ce H¢ ¢ CH₂(d).

Bor H₂C Y CH3 (Transition state) Step I step2 Energy? (Intermedidteie.cambocation) c hal Energy Me Reactant Reactants Product

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