Chapter 2: Problem 27
Which of the following compounds can exhibit geometrical isomerism? (a) \(\mathrm{IBrC}=\mathrm{CFCI}\) (b) Cinnamic acid (c) Benzophenone oxime (d)
Chapter 2: Problem 27
Which of the following compounds can exhibit geometrical isomerism? (a) \(\mathrm{IBrC}=\mathrm{CFCI}\) (b) Cinnamic acid (c) Benzophenone oxime (d)
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Get started for freeDirections: This section contains 1 paragraph. Based upon the paragraph, 3 multiple choice questions have to be answered. Each question has 4 choices (a), (b), (c) and (d), out of which ONLY ONE is correct. Passage I Alkenes undergo a variety of reactions like hydrogenation, halogenation, oxidation, epoxidation and so on. The double bond of the alkenes acts as electron donor. An unsaturated hydrocarbon gave, on treatment with alkaline \(\mathrm{KMnO}_{4}\) under hot conditions, one mole of adipic acid. The unsaturated hydrocarbon could be (a) \(\mathrm{H}_{3} \mathrm{C}-\mathrm{C} \equiv \mathrm{C}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{CH}_{3}\) (b) \(\mathrm{H}_{3} \mathrm{C}-\mathrm{CH}_{2}-\mathrm{C} \equiv \mathrm{C}-\mathrm{CH}_{2}-\mathrm{CH}_{3}\)
Four reagents and specific reactions in which they are involved are given. Identify the wrongly matched option among the following (a) Hot alcoholic KOH \(-\) dehydrohalogenation (b) \(\mathrm{H}^{+} / \mathrm{H}_{2} \mathrm{O}\) - hydration (c) \(\mathrm{H}^{+} / \Delta\) - dehydration (d) Unsymmetrical alkene - anti Markovnikov addition
Identify the incorrect statement among the following (b) The dipole moment of \(\mathrm{CH}_{2} \mathrm{Cl}_{2}\) is greater than that of \(\mathrm{CH}_{3} \mathrm{Cl}\). (c) The cis isomers become increasingly less stable as the size of the \(\mathrm{R}\) groups increase. (d) Alkenes with two identical groups on the same doubly bonded carbon have no geometrical isomers.
Which of the following compounds on reductive ozonolysis will give two molecules of \(\mathrm{CH}_{2}(\mathrm{CHO})_{2} ?\) (a) 1,3 -cyclohexadiene (b) 2,4 -hexadiene (c) 1,4 -cyclohexadiene (d) 1-Methyl-1,3-cyclopentadiene
\(\mathrm{CH}_{3}-\mathrm{CH}=\mathrm{CH}_{2}+\mathrm{Br}_{2} \rightarrow(\mathrm{A}) \stackrel{\mathrm{NaNH}_{2}}{\longrightarrow}(\mathrm{B}) \stackrel{\mathrm{H}^{+}}{\longrightarrow}(\mathrm{C}) .\) The structure of (C) is (a) \(\mathrm{CH}_{3} \mathrm{C} \equiv \mathrm{CH}\) (b) \(\mathrm{H}_{3} \mathrm{C}-\mathrm{C} \equiv \mathrm{C}-\mathrm{CH}_{3}\) (c) \(\mathrm{BrCH}_{2}-\mathrm{CH}_{2}-\mathrm{CH}_{2} \mathrm{Br}\) (d) \(\mathrm{H}_{2} \mathrm{C}=\mathrm{C}=\mathrm{CH}_{2}\)
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