An alkene ‘A’ (Mol. formula `C_5H_(10)` )on ozonolysis gives a mixture of two compounds ‘B’ and ‘C’. Compound ‘B’ gives positive Fehling’s test and also forms iodoform on treatment with `I_2` and NaOH. Compound ‘C’ does not give Fehling’s test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.

An alkene 'A' (molecular formula C_(5)H_(10) ) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatement with I_(2)" and "NaOH . Compound 'C' does not give Fehling's test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.

The following compounds will give positive Fehling’s test.

The compound that gives both iodoform and Fehlings test is :

Which of the following compounds will give positive iodoform test with I_(2) and NaOH ?

Which of the following compounds will give iodoform test with I_(2)//NaOH

A compound containing molecular formula C_(5)H_(10)Cl_(2) on hydrolysis gives compound containing molecular formula C_(5)H_(10)O , which reacts with NH_(2)OH and also forms iodoform but does not give Fehling test original compound is

A compound (A) with molecular formula C_4H_10O on oxidation forms compound (B). The compound (B) gives positive iodoform test and on reaction with CH_3MgBr followed by hydrolysis gives (C). Identify . A, B and C and give the sequence of reactions.