Chapter 1: Problem 132
The IUPAC name of \(\quad 1\) is
Chapter 1: Problem 132
The IUPAC name of \(\quad 1\) is
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Get started for freeArrange the acids (I-V) listed below in the decreasing order of their acid strength and justify. (i) Butanoic acid (ii) Trichloro acetic acid (iii) Chloroacetic acid (iv) Trimethyl acetic acid (v) Bromo acetic acid
Statement 1 Stereoisomers with D-configuration and L-configuration do not refer to compounds with \((+)\) and \((-)\) rotation respectively. and Statement 2 The letters \(\mathrm{D}\) and \(\mathrm{L}\) refer to the configuration of atoms or groups at a chiral centre based on \(\mathrm{D}\) and \(\mathrm{L}\) glyceraldehydes.
The compound which has only one isopropyl group is (a) \(2,2,2,3\) -tetramethyl pentane (b) 2,4 -dimethyl pentane (c) \(2,2,3\) -tri methyl pentane (d) 2 -methyl pentane
\(\mathrm{pK}_{\mathrm{a}}\) value is least for (a) \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\mathrm{COOH}\) (b) \(\mathrm{BrCH}_{2}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{COOH}\) (c) \(\mathrm{CH}_{3}-\mathrm{CCl}_{2}-\mathrm{COOH}\) (d) \(\mathrm{CH}_{3}-\mathrm{CHCl}-\mathrm{COOH}\)
The isomeric cis \(-2\) -butene and trans 2 -butene differ in (a) the products obtained by addition of \(\mathrm{HBr}\) (b) their reduction products on hydrogenation (c) their products on ozonolysis (d) the products they give on bromine addition
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