Among the carboxylic acid shown below, the ones that exhibit stereoisomerism and also form, cyclic anhydrides on heating are
I. HOOCCH(CH₃)CH₂CH₂COOH
II. HOOCCH(C₃H₇)COOH
III. HOOCCH(C₂H₅)CH₂COOH
IV. HOOCC(CH₃)(C₂H₅)COOH

A. CH₃C$${\text{O}}_2^ - $$ > CH₃O^- > C₆H₅O^- > N$${\text{O}}_3^ - $$ B. CH₃O^- > N$${\text{O}}_3^ - $$ > C₆H₅O^- > CH₃C$${\text{O}}_2^ - $$ C. CH₃O^- > C₆H₅O^- > CH₃C$${\text{O}}_2^ - $$ > N$${\text{O}}_3^ - $$ D. C₆H₅O^- > CH₃O^- > N$${\text{O}}_3^ - $$ > CH₃C$${\text{O}}_2^ - $$

A. (i) peracid, (ii) H⁺, (iii) Zn/dil.HCl B. (i) Alkaline KMnO₄, (ii) NalO₄, (iii) N₂H₄/KOH C. (i) Alkaline KMnO₄, (ii) H⁺, (iii) Zn/dil.HCl D. (i) O₃/Me₂S, (ii) NaOEt, (iii) N₂H₄/KOH

A. CH₃CO₂H B. CH₃CONHC₆H₅ C. n-C₆H₁₃C ≡ CH D. n-C₆H₁₃CHO

A. reaction with sodium cyanide in the presence of nickel catalyst B. reaction with chloroform and sodium hydroxide C. diazotisation followed by reaction with CuCN D. reaction with ethyl formate followed by thermolysis