Compound A on ozonolysis gives acetone and glyoxal. The compound A is
2, 5-dimethyl hex-2, 4-dene
2, 5-dimethyl hex-1, 5-diene
2, 5-dimethyl hex-3, 4-diene
2, 5-dimethyl but-2, ene
, A and B are
alc KOH and SeO2
NaNH2 and lindlar catalyst
alc KOH and NaNH2
Lindlar catalyst and NaNH2
C.
alc KOH and NaNH2
Acetylene homologues isomense when heated with ethanohc KOH, the triple bond moving towards the centre of the chain.
When alkynes are heated with sodamide in an inert solvent [paraffin), triple bond shifts
towards the end of the chain.
Which compound does not form 2-methyl but-2-ene on heating with alc. KOH?
1-bromo-2 methyl propane
2-bromo-3-methyl butane
2-bromo-2-methyl butane
None of the above
The olefin which on ozonolysis gives CH3CH2CHO and CH3CHO is
2-butene
1-pentene
1-butene
2-pentene
Which one of the following alkenes will react faster with H2 under catalytic hydrogenation conditions?
Liquid hydrocarbon is converted into mixture of gaseous hydrocarbons by
cracking
oxidation
hydrolysis
distillation under reduced pressure
Which of the following is the most reactive towards ring nitration?
Benzene
Toluene
Mesitylene
m-xylene
Compounds (A) gives two mol acetone and glyoxal on ozonolysis?
2, 5-dimethyl hexyne
2, 5-dmethyl hex-3-ene
2, 5-dimethyl hex-2-yne
2, 5-dimethyl hexa-2, 4-diene