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Reaction intermediate#!#carbocation

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Reaction Mechanism : transition state - reaction intermediates, carbocation - rearrangement and hydride shift

CH_3-underset(CH_3)underset(|)(CH)-underset(CH_3)underset(|)overset(CH_3)overset(|)(C )-CH_2Br underset(HOH)overset(NaOH)(rarr) Consider the following statement for the given reaction 1. The reaction is S_N1 2. The reaction intermediate is carbocation 3. The major product will be 2,3-dimethyl-3-pentanol 4. The major product has one stereogenic centre

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Introduction To Organic Chemistry - Reaction Intermediates - Carbocation

Reaction Intermediates|| Carbocation|| Stability OF Carbocation|| Rearrangement OF Carbocation (Hydride, Alkyl and Phenyl shift Reaction)

Acid catalysed hydration of alkene give alcohol. In thic reaction addition of water takes place according to Markownikov's rule. Since intermediate carbocation is formed in this reaction, rearrangment of carbocation takes place. In oxymercuration-demercuration reaction hydration of alkene takes place according to markownikov's rule. Oxymercuratio-demercuration-dermercuration no rearrangement is possible. in hydroboration-oxidation hydration of alkene takes place according to anti marjownikow's addition. in HBO reaction rearrangement is not possible. both in oxymercuration-demercuation and hydroboration-oxidation, intermediate carbocation are not formed. Q. The product formed in the following reaction is: Pruduct

Acid catalysed hydration of alkene give alcohol. In thic reaction addition of water takes place according to Markownikov's rule. Since intermediate carbocation is formed in this reaction, rearrangment of carbocation takes place. In oxymercuration-demercuration reaction hydration of alkene takes place according to markownikov's rule. Oxymercuratio-demercuration-dermercuration no rearrangement is possible. in hydroboration-oxidation hydration of alkene takes place according to anti marjownikow's addition. in HBO reaction rearrangement is not possible. both in oxymercuration-demercuation and hydroboration-oxidation, intermediate carbocation are not formed. Q. CH_(3)-C-=C-Hunderset(H_(2)O_(2)//OH^(-))overset((Sia)_(2)HB)toA, A is