EASY
Earn 100

Which of the following molecules gives 'Glyoxal' as one of the product on reductive ozonolysis?

50% studentsanswered this correctly

Important Questions on Unsaturated Hydrocarbons- Alkenes

HARD
A single compound of the structure

Question Image

is obtainable from ozonolysis of which of the following cyclic compounds?
MEDIUM

The product of which of the following reactions forms a reddish brown precipitate when subjected to Fehling's test? 

MEDIUM
The compound which on ozonolysis produces a mixture of propanone and ethanal is;
EASY
An olefin is treated with ozone and then with zinc and water. The products obtained are Ethanal and propanone. The olefin will be
EASY
Which of the following compound, on ozonolysis, gives an aldehyde and a ketone?
MEDIUM
An alkene gives two moles of HCHO, one mole of CO2 and one mole of CH3COCHO on ozonolysis. What is its structure ?
MEDIUM
Olefin A gives 2 moles acetone and one mole glyoxal on ozonolysis. The structure of A
HARD

Compound P and R upon ozonolysis produce Q and S, respectively. The molecular formula of Q and S is C8H8O . Q undergoes Cannizzaro reaction but not haloform reaction, whereas S undergoes haloform reaction but not Cannizzaro reaction.

Question Image

Question Image​​​​​​​

MEDIUM
An unsaturated hydrocarbon X absorbs two hydrogen molecules on catalytic hydrogenation, and also gives following reaction:
XiiZnH2OiO3AAgNH32+B  (3-oxo-hexanedicarboxylic acid) X will be:
MEDIUM
An organic compound 'A' C4H8on treatment with KMnO4/H+ yields compound 'B' C3H6O. Compound 'A' also yields compound 'B' an ozonolysis. Compound 'A' is :
EASY
The major product formed when 2-butene is reacted with O3 followed treatment with Zn/H2O  is
HARD

Identify the major product in the following reaction

Question Image

HARD
An unsaturated hydrocarbon X on ozonolysis gives A. Compound A when warmed with ammoniacal silver nitrate forms a bright silver mirror along the sides of the test tube. The unsaturated hydrocarbon X is :
HARD
The reaction sequence(s) that would lead to o-xylene as the major product is(are)
MEDIUM
The reaction of an alkene X with bromine produces a compound Y, Which has 22.22%C, 3.71%H, 74.07%Br. The ozonolysis of alkene X gives only one product. The alkene X is [Given : atomic mass of C=12; H=1; Br=80]
MEDIUM
The products obtained by the ozonolysis of 2 -methylbut- 1 -ene are
HARD
Which compound would give 5-keto-2-methyl hexanal upon ozonolysis?