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JEE CHEMISTRY MCQ: HYDROCARBONS

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Bromination of toluene gives

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Correct option: C

Mixture of

\mathrm{o}

and

\mathrm{p}

substituted product

Option C is correct because the methyl group (

\mathrm{-CH}_3

) in toluene is an ortho- and para-directing group, leading to a mixture of ortho- and para-substituted products.

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\mathrm{Ca}{\mathrm{C}_2} + {\mathrm{H}_2}\mathrm{O} \to X\xrightarrow{{{\mathrm{O}_3}/\frac{{{\mathrm{H}_2}\mathrm{O}}}{{\mathrm{O}{\mathrm{H}^ + }}}}}\mathrm{HCOOH} + \mathrm{HCOOH},X\;\mathrm{is}

In benzene, there is a delocalisation of π-electrons. Hence, each π-electron is attached by….carbon nuclei. Which statement is false? Assertion (A) In comparison to ethyl chloride, it is not easy to carry outnucleophilic substitution on vinyl chloride.

Reason (R) Vinyl group is an electron donating. If 2-oxopropanal and methanal are obtained by the reductive ozonolysis of compound (A), then the number of

\sigma

-bonds presents in Fischer-Tropsch process is used in the manufacture of: