Chapter 1: Problem 66
The specific arrangement of atoms that characterize a particular stereoisomer is known as (a) tautomer (b) conformation (c) configuration (d) geometry
Chapter 1: Problem 66
The specific arrangement of atoms that characterize a particular stereoisomer is known as (a) tautomer (b) conformation (c) configuration (d) geometry
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Get started for freeThe specific rotation of a pure optically active compound is \(+12^{\circ} .\) The specific rotation of the sample in a reaction with \(20 \%\) racemization and \(80 \%\) retension of configuration will be (a) \(+12^{\circ}\) (b) \(-12^{\circ}\) (c) \(+9.6^{\circ}\) (d) \(-2.4^{\circ}\)
The maximum number of isomers for the compound with molecular formula C IBrClF is (a) 4 (b) 5 (c) 6 (d) 7
In benzene all the \(\mathrm{C}-\mathrm{C}\) bonds are of equal length because of (a) resonance (b) aromaticity (c) hyperconjugation (d) tautomerism
The IUPAC name of \(\mathrm{CH}_{3}-\mathrm{CO}-\mathrm{CHCl}-\mathrm{CH}_{2}-\mathrm{COOH}\) is (a) 3-Chloro-4-oxopentanoic acid (b) 4-Oxo-3-Chloropentanoic acid (c) 2-Oxo-3-Chloropentanoic acid (d) 1 -Carboxy-3-Chloro-4-ketobutane
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) \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}<\mathrm{CH}_{3}-\mathrm{CH}_{2}-<\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\)
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