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The reaction of propene with HOCl proceeds via the addition of –

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Important Questions on Hydrocarbons

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In the given reaction, the product P is

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Given,

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The enthalpy of hydrogenation of these compounds will be in the order as:
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The reaction of C6H5CH=CHCH3 with HBr produces:
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3-Methyl-pent-2-ene on reaction with HBr in presence of peroxide forms an addition product. The number of possible stereoisomers for the product is
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The major product of the following reaction is:

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The major product of the following reaction is:

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A single compound of the structure

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is obtainable from ozonolysis of which of the following cyclic compounds?
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Compound(s) that on hydrogenation produce(s) optically inactive compound(s) is (are)
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In the reaction with HCl, an alkene reacts following the Markovnikov's rule to give the product 1-chloro-1-methylcyclohexane. The possible reaction of the alkene is
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What is the major product expected from the following reaction?

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Where D is an isotope of hydrogen.

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The maximum number of isomers that can result from mono bromination of 2-methyl-2-pentene with N - bromosuccinimide in boiling CCl4 is
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The major product of the following reaction is:
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The reaction of propene with HOCl Cl2+H2O proceeds through the intermediate:
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The correct structure of the product A formed in the reaction is

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In the following reactions, the product S is


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The correct statement(s) for the following addition reactions is(are)

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In the following reaction, the major product is
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A compound A with molecular formula C10H13Cl, gives a white precipitate on adding silver nitrate solution. A on reacting with alcoholic KOH gives compound B as the main product. B on ozonolysis, gives C and D. C gives Cannizaro reaction, but not aldol condensation. D gives aldol condensation, but not Cannizaro reaction. A is
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The major product in the following conversion is

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Which compound would give 5-keto-2-methyl hexanal upon ozonolysis?