Ozonolysis of an alkene A yields two moles of me,thanol and one mole of ethane-1, 2 di al. Give the structure of A and IUPAC name.

An alkene 'A' upon ozonolysis gives a mixture of ethanal and pentan-3-one write the structure and IUPAC name of 'A'

An alkene A on ozonolysis gives a mixture of ethanal & pentan-3-one. Write structure & pentan-3- one. Write structure & IUPAC name of A.

Monomer A of a natural polymer on complete ozonolysis yields two moles of CH_3COCHO . Deduce the structure of A.

An alkene which on ozonolysis forms one molecule of glyoxal and 2 molecules of formaldehyde. Give its structure and name the compound.

A hydrocarbon containing two double bonds gave on reductive ozonolysis ethanal, glyoxal and propanone. Predict the structure of the hydrocarbon and give its IUPAC name.

An organic compound A( C_3H_8O ) on treatment with Cu dust at 573K gives B. B does not reduce Fehling's solution but gives a yellow precipitate of compound C with I_2//NaOH . Deduce the structures of A , B and C and their IUPAC names.

One mole of symmetrical alkene upon ozonolysis gives two moles of an aldehyde having the molecular mass 44 u . Predict the alkene.

A gaseous hydrocarbon decolourise bromine in C""Cl_4 . One molecule of acetone and one molecule of acetaldehyde are obtained as a result of its ozonolysis. Determine the structural formula of the compound and write its IUPAC name. Give all reactions involved.

The hydrocarbon A, adds one mole of hydrogen in the presence of a platinum catalyst to form n-hexane . When A is oxidised vigorouslty with KMnO_4 , a single carboxylic acid, containing three carbon atoms , is isolated. Give the structure of A and explain.