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Asked Nov 26, 2019
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What is the synthesis and mechanism for the following?

Finish the syntheses to afford (result in) the desired products as the major product:
?
alkyl chloride
?
alkyl chloride
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Finish the syntheses to afford (result in) the desired products as the major product: ? alkyl chloride ? alkyl chloride

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Step 1

Hofmann's Rule: It is elimination reaction in which the formation of alkene from rather most unhindered (least substituted) β-hydrogen elimination.

 Saytzeff'...

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Synthesis of the given alkene is shown below, CI MEOH NaOEt It is elimination reaction, sodium ethoxide is used as a base, it abstract the proton from hindered carbon forms carbanion followed by elimination of chlorine gives most hindered or highly substituted alkene (Saytzeffs product) The mechanism of the reaction is shown below, Saytzeff's Rule CI МеОн H NaOEt

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