Fischer's Esterification Process
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An organic compound (A) (molecular formula (C8H16O2) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and alcohol (C). Oxidation of (C) with chromic acid produced (B). (C) on dehydration gives but - 1 - ene. Write equations for the reactions involved.
Give plausible explanation for each of the following:
Cyclohexanone forms cyanohydrin in good yield but 2, 2, 6-trimethyl cyclohexanone does not.
These are two −NH2 groups in semicarbazide. However, only one is involved in the formation of semicarbazones.
During the preparation of esters from a carboxylic acid and an alcohol in the presence of an acid catalyst, the water or the ester should be removed as soon as it is formed.
- Reduce the acid with LiAlH4.
Convert the acid to an acid chloride, and react the acid chloride with water.
- Convert the acid to an acid chloride, and reduce the acid chloride with lithium aluminium tri(t-butoxy) hydride.
- Convert the acid to an acid chloride, react the acid chloride with a Grignard reagent, and reduce the product with LiAlH4.
- Primary amines are less basic than the secondary amines.
- Primary amines on treating with nitrous acid solution form corresponding alcohols except methyl amine.
- Primary amines can be prepared by the Gabriel phthalimide synthesis.
- The intermolecular association in primary amines is less than the intermolecular association in secondary amines
- Acetyl chloride
- Acetic anhydride
- Phenyl acetate
- Benzoyl chloride
- Alkaline KMnO4
- BH3, THF/NaOH, H2O2
- O3/Zn dust
- OsO4/NaHSO3, H2O
- Alcohol with hydrogen in presence of palladium
- Alcohol with LiAlH4
- Aldehyde with LiAlH4
- All of the above
- Al2O3 at 250∘C
- conc. H2SO4 at 170∘C
- conc. H2SO4 at 140∘C
- Al2O3 at 350∘C
- P is an aldehyde whereas Q is a carboxylic acid.
- P is a carboxylic acid whereas Q is a ketone.
- P is and Q both are aldehydes.
- P is and Q both are carboxylic acids.
\( A +\frac{ Br \text { (entess) }}{ H _{2} O } \) \( \frac{ Br _{2}}{ CS _{2}, 5^{\circ} C }= B \)
- FeCl3
- AlCl3
- NH3
- FeBr3
- Phenyl salicylate
- Methyl salicylic acid
- Acetyl salicylate
- Acetyl salicylic acid
How many reactions are correct?
- CH3−CH2−OH+HI⟶CH3−CH2−I+H2O
- CH3−(CH3)CH−OH+HI⟶CH3−(CH3)CH−I+H2O
- CH3−(CH3)2C−OH+HI⟶CH3−(CH3)2C−I+H2O
- All of the above
- CH3CH2COOCH(CH3)CH2CH3
- CH3CH2COOC(CH3)2CH2CH3
- CH3CH2COOC2H5
- CH3CH2COOC6H5
CH3−CH2−CH2−O−CH3+HBr→
- Bromopropane and methanol
- Bromomethane and propanol
- Ethanol and bromoethane
- None
(i) Formaldehyde and acetaldehyde
(ii) Dimethyl ether and ethyl alcohol
- Aldehyde
- Ketone
- Benzene
- Propene