Chapter 1: Problem 133
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Chapter 1: Problem 133
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The specific arrangement of atoms that characterize a particular stereoisomer is known as (a) tautomer (b) conformation (c) configuration (d) geometry
A bond that undergoes heterolytic cleavage most readily is (a) \(\mathrm{C}-\mathrm{C}\) (b) \(\mathrm{O}-\mathrm{H}\) (c) \(\mathrm{C}-\mathrm{O}\) (d) \(\mathrm{C}-\mathrm{H}\)
which among the following compounds can exhibit geometrical isomerism? (a) 2 -phenyl but- 1 -ene (b) 1 -phenyl but- 2 -ene (c) 3 -phenyl but-1-ene (d) 1,1 -dichlorobut- 1 -ene
The correct increasing order of electron donating effect of \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-,\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}-\) and \(\mathrm{CH}_{3}-\mathrm{CH}_{2}-\) groups when attached to benzene or unsaturated system is (a) \(\mathrm{CH}_{3}-\mathrm{CH}_{2}-<\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}-<\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\) (b) \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-<\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}-<\mathrm{CH}_{3}-\mathrm{CH}_{2}-\) (c) \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}-<\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-<\mathrm{CH}_{3}-\mathrm{CH}_{2}-\) (d) \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}<\mathrm{CH}_{3}-\mathrm{CH}_{2}-<\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\)
The incorrect resonance structure of diazomethane is (a) \(\mathrm{H}_{2} \stackrel{\ominus}{\cdots}-\mathrm{N} \equiv \cdots\) (b) \(\mathrm{CH}_{3}-\mathrm{N}=\cdots \mathrm{N}\) (c) \(\mathrm{H}_{2} \mathrm{C}=\stackrel{\oplus}{\mathrm{N}}=\cdots \mathrm{N}^{\cdot}\) (d) \(\mathrm{H}_{2} \mathrm{C} \rightarrow \ddot{\mathrm{N}}=\cdots^{\ominus}\)
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