An alkene (A) with molecular formula `C_(5)H_(10)` undergoes ozonolysis to form two aldehydes "(X)" and "(Y)" in which "(X)" contains four carbon atoms.Another "alkene (B) which is an isomer of (A) undergoes ozenolysis to form two aldehyde (C) and (D) in which (C) contain "3" carbon atoms.Identify "(X),(Y),(A)," (B) , (C) and (D).Write the reactions involved

An alkene of the molecular formula C_(6)H_(12) on reductive ozonolysis give two different aldehydes as products.How many alkenes including stereoisomers satisfy this criterion?

An organic compound (X) undergoes acid hydrolysis to form two compound (Y) and (Z). The compound (Y) reacts with sodium carbonate to form (A) which when heated with soda lime forms (B) which is CH_(4) . The compounds (Y) on reduction with LiAIH_(4) forms (Z.) Identify X,Y,Z,A,B and write the reactions involved.

How many structural isomers are possible for the molecular formula C_(4)H_(8) which can undergo ozonolysis ?

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.

A hydrocarbon (A) of the formula C_(7)H_(12) on ozonolysis gives a compound (B) which undergo aldol condensation giving 1-acetylcyclopentene. Identify (A) and (B).

Hydrocarbon (X), C_(7)H_(12) , on reaction with boron hydride followed by treatment with CH_(3)COOH yields (A). On reductive ozonolysis (A) yields a mixture of two aldehydes, (B) and (C ). Of these, only (B) can undergo Cannizzaro reaction. (A) exists in two geometrical isomer, (A-1) and (A-2) , of which (A-2) is more stable. Gives structures of (X), (A), (B), (C ), (A-1) , and (A-2) with proper reasoning.