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Balance the following equation in acidic conditions. Phases are optional. Cu NO3,
1 answer:
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Answer:
None of these
Explanation:
Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.
Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :
Step -1 : Generation of stable carbocation.
Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.
Step-2: Attack of the ring to the carbocation
The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.
The product formed is shown in mechanism does not mention in any of the options.
So, None of these is the answer
Answer:
Major product does not undergo oxidation since it is a tertiary alcohol whereas minor product undergoes oxidation to ketone as it is secondary alcohol.
Explanation:
Hello,
In this case, given the attached picture, the hydration of the 1 methylcyclohexene yields to alcohols; 1-methylcyclohexan-1-ol and 1-methylcyclohexan-2-ol. Thus, since the OH in the 1-methylcyclohexan-1-ol (major product) is bonded to a tertiary carbon (bonded with other three carbon atoms) it is not able to increase the number of oxygen bonds (oxidation) as it already attained the octet whereas the 1-methylcyclohexan-2-ol (minor product) is able to undergo oxidation to ketone as the carbon bonded to it is secondary (bonded with other two carbon atoms), so one extra bond the oxygen is allowed to be formed to carbonyl.
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