Alkenes

Compound X is

Which compound would give 5 - keto - 2 - methyl hexanal upon ozonolysis ?

A compound A with molecular formula $\ce{C10H13Cl}$ gives a white precipitate on adding silver nitrate solution. A on reacting with alcoholic KOH gives compound B as the main product. B on ozonolysis gives C and D. C gives Cannizaro reaction but not aldol condensation. D gives aldol condensation but not Cannizaro reaction. A is :

What is the major product expected from the following reaction ?

1-Methylcyclopentene $\xrightarrow{\text{D}-\text{Cl}}$

Where D is an isotope of Hydrogen.

In the hydroboration - oxidation reaction of propene with diborane, $\ce{H2O2}$ and NaOH, the organic compound formed is :

In allene ($\ce{C3H4}$), the type(s) of hybridization of the carbon atoms is (are):

The gas liberated by the electrolysis of Dipotassium succinate solution is :

$\ce{C6H5-CH2-CH=CH2}$ on mercuration-demercuration produces the major product :

In the presence of peroxide, HCl and HI do not give anti-Markownikoff's addition to alkenes because :

The total number of carboxylic acid groups in the product P is

Compounds formed from P and Q are, respectively

Match the chemical conversions in List I with the appropriate reagents in List II and select the correct answer using the code given below the lists:

The number of optically active products obtained from the complete ozonolysis of the given compound is

The structure of compound P is

In the reaction shown below, the total number of possible intramolecular aldol condensation products formed from Y is

The structures of the products Q and R, respectively, are

Compound H is formed by the reaction of

Cyclohexene on ozonolysis followed by reaction with zinc dust and water gives compound E. Compound E on further treatment with aqueous KOH yields compound F. Compound F is

The number of stereoisomers obtained by bromination of trans-2-butene is