write the products and probable mechanism of the reaction: CH3Br+ aq.KOHof
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CH3BR+KOH=CH3OH+KBR.........
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The reaction will follow the nucleophilic substitution reaction.
Explanation:
Methyl bromide is a primary haloalkane and it will undergo nucleophilic substitution by mechanism. It takes place in a single step.
The aqueous KOH is a strong base, here the OH will act as a nucleophile and attack the methyl bromide.
When alkyl halides are treated with aqueous KOH, the halogen is substituted by OH, yielding alcohol.
Following the above point, the reaction will be
→
This reaction and mechanism are used in the production of alcohol.
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