Question

An organic compound a, c6h10o, on reaction with ch3mgbr followed by acid treatment gives compound b, which on ozonolysis gives compound

c. c in presence of a base gives 1-acetyl cyclopentene

d. the compound b on reaction with hbr gives compound

e. write the structures of compounds a, b, c and

e. show how d is formed from c

Answer 1

"of" (and any subsequent words) was ignored because we limit queries to 32 words. 

Answer 2

Answer:

2 CH₃COOH + 2 Na ⇒  2 CH₃COONa + H₂ ↑

      ( A )                                   ( B )

CH₃COOH + C₂H₅OH ⇒  CH₃COOC₂H₅ + H₂O

                        ( C )                 ( D )

CH₃COOC₂H₅ + NaOH  ⇒ C₂H₅OH + CH₃COONa

Therefore we identified

A - CH₃COOH

B - CH₃COONa

C - C₂H₅OH

D - CH₃COOC₂H₅