The reagent with which both acetaldehyde and acetone react is
Fehling's solution
I2/ NaOH
Tollen's reagent
carbonic acid
Which of the following gives an aldehyde on dry distillation?
Calcium formate + calcium acetate
Calcium acetate + calcium benzoate
Calcmm acetate
Calcium benzoate
The IUPAC name of
2-methyl-3-bromohexanal
3-bromo-2-methylbutanal
2-methyl-3-bromobutanal
3-bromo-2-methylpentanal
An organic compound 'A' burns with a sooty flame. It is negative towards Tollen's reagent test and positive for Borsche's reagent test. The compound 'A' is
acetophenone
acetone
salicylic acid
benzaldehyde
IUPAC name of H3C—(OH)CH—CH2—CHCOOH—CH3 is
4-hydroxy-1-methyl pentanoic acid
4-hydroxy-2-methyl pentanoic acid
2-hydroxy-4-methyl pentanoic acid
2-hydroxy-2-methyl pentanoic acid
The relative acidic strengths of benzoic acid, o-toluic acid and p-toluic acid is of the decreasing order
o-toluic acid > p-toluic acid > benzoic acid
p-toluic acid > benzoic acid > o-toluic acid
o-toluic acid > benzoic acid > p-toluic acid
p-toluic acid > o-toluic acid > benzoic acid
Conversion of benzene to acetophenone can be brought by
wurtz reaction
wurtz- fittig's reaction
Fridel crafts alkylation
Friedel crafts acylation
D.
Friedel crafts acylation
Benzene on treatment with a carboxylic acid chloride or anhydride in the presence of anhydrous AlC3, forms aliphatic-aromatic ketones. The reaction is known as Friedel-Crafts acylation.
The compound formed when calcium acetate and calcium formate is distilled
acetone
acetaldehyde
benzaldehyde
acetophenone
Acetone and propanal are
functional isomers
position isomers
geometrical isomers
optical isomers