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JEE CHEMISTRY MCQ: HYDROCARBONS
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The decreasing order of reactivity of hydrogen bromide on the following alkenes is
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Correct option: B
IV II I III
The correct answer is B (IV II I III) because the reactivity of alkenes with HBr increases with the stability of the carbocation formed, and is decreased by electron-withdrawing groups.
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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 -bonds presents in Fischer-Tropsch process is used in the manufacture of:
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 -bonds presents in Fischer-Tropsch process is used in the manufacture of:
