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An organicacid (A) (C_(5)H_(10)O_(2)) reacts with Br_(2)in presenceof phosphorus to give (B). Compound(B) containsan asymmetriccarbon atom and yields(C). Ondehydrohalogention, compound (C) doesnot showgeometricisomersim andon decarboxylationgivesan alkene (D) whichon ozonlysis isomerism and on decarboxylation givesan alkene (D) whichon ozonolysis give (E) and (F). Compound (E) givesa positive Schiff'stest but (F) doesn 't. Give structures of (A) to (F) with reasons. |
Answer» Solution :(E) is aldehydeand (F) is ketone .The NUMBEROF C-atom in (A). (B) and (C) are5andin (D) justfour. It.salsoclear that (A) hasattlesat ONE `alpha` - hydrogenas ITIS showingHVZreaction . Twooptionsare possiblefor (A). ![]()
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