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1-bromo-1-methylcyclohexane

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13y ago
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1-bromo-3-methylcyclohexane is the major monobrominated product formed when methylcyclohexane undergoes free radical bromination. This occurs because the bromine radical prefers to attack the tertiary carbon due to its greater stability compared to primary or secondary carbons.

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Q: The major monobrominated product which results when methylcyclohexane is subjected to free radical bromination is?
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Is toluene will under go bromination?

Yes, toluene will undergo bromination. When treated with bromine in the presence of a Lewis acid catalysts such as FeBr3 or AlBr3, toluene will undergo electrophilic aromatic substitution to form bromotoluene as the major product.


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A possible reason for low yield in the bromination of acetanilide could be the presence of impurities in the starting material. Impurities can compete for reaction sites or react in unwanted ways, leading to lower yields of the desired product. It is important to start with a pure sample of acetanilide to maximize the yield of the bromination reaction.


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Why in bromination of acetanilide using bromine in acetic acid give para bromoacetanilide as major product?

Steric hindrance from the bulky acetanilide group directs the electrophilic bromination to the para position, as it is the least hindered position for bromine attack. This leads to the formation of para-bromoacetanilide as the major product.

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Why in bromination of acetanilide using bromine in acetic acid give para bromoacetanilide as major product?

Steric hindrance from the bulky acetanilide group directs the electrophilic bromination to the para position, as it is the least hindered position for bromine attack. This leads to the formation of para-bromoacetanilide as the major product.


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