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The major monobrominated product which results when methylcyclohexane is subjected to free radical bromination is?
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1-bromo-1-methylcyclohexane
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∙ 13y ago
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Is toluene will under go bromination?
Yes U will take bromine in ccl4 in presence of benzoyl peroxide u will get mono bromination product. Type your answer here...
Why in bromination of acetanilide using bromine in acetic acid give para bromoacetanilide as major product?
The -NHCOR group is less powerfully activating then the -NH2 group. In addition, the degree of steric hindrance is much greater in the case of a -NHCOR group, such as is found in acetanilide. This results in the compound being much more para directing. For an example, see Morrison and Boyd 's text "Organic Chemistry", sixth edition, Page 848.
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Is toluene will under go bromination?
Yes U will take bromine in ccl4 in presence of benzoyl peroxide u will get mono bromination product. Type your answer here...
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Adding halogens to alkene groups (X2) requires that the product adopt an anti configuration. Hexene will also lose its double bond upon bromination. Benzene is energetically unfavorable when a reaction attempts to break its double bond. The resonance benzene has makes it very stable, and thus very hard to break.
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CH3CH2CH3 + Br2 = CH3CHBrCH3 + HBr The major product formed from the reaction is 2-bromopropane. It is a free radical bromination reaction. It is called a substitution reaction because you are substituting a H an atom for a Br atom and making HBr.
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Why in bromination of acetanilide using bromine in acetic acid give para bromoacetanilide as major product?
The -NHCOR group is less powerfully activating then the -NH2 group. In addition, the degree of steric hindrance is much greater in the case of a -NHCOR group, such as is found in acetanilide. This results in the compound being much more para directing. For an example, see Morrison and Boyd 's text "Organic Chemistry", sixth edition, Page 848.
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