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Wednesday, January 29, 2020

Highly branched carboxylic acids are less acidic than unbranched acids. Explain why?


The carboxylate ion of the branched chain acids is shielded from solvent molecules and thus resists for resonance whereas unbranched acids having lesser solvation effect shows resonance stabilized anion to show more acidic character.

What is Dunstan's test , How can it use for test Glycerol ?

When phenolphthalein is added to dilute cold solution of borax, a pink colour is produced. When glycerol is mixed in it, in cold, the colour disappears, but on heating colour reappears. It is a characteristic test of glycerol. This test is called Dunstan's test.

Related Questions:

Both glucose and fructose are reducing sugars but sucrose is non-reducing in nature. Why?
Fructose contains a keto group, yet it reduces Fehling solution and Tollen's reagent. Why ?
What is Dunstan's test , How can it use for test Glycerol ?
What is luca's reagent and where is luca's reagent uses ?
What is Victory-Meyer's test and how can distinction between 1°, 2° and 3° alcohols by this ?
Benzaldehyde gives a positive test with Tollen's reagent but not with Benedict's and Fehling's solution. Comment why?
Aromatic amines are lesser basic than aliphatic amines.why ?
Which are the compounds gives positive Tollen's test?
What is Tollen's reagent?
What is Carbylamine test or Isocyanide test ?
What is Hinsberg's reagent and where Hinsberg's test use?
N-Ethyl-N-methyl propanamine does not show optical activity why?


Carbonyl compounds do not undergo nucleophillc substitution reactions.why?


Nucleaphilic substitution reactions, at the minimum H-(hydride) ion from aldehydes and -CH3 from ketones needs to be withdrawn. These are strong nucleophiles, and can not be displaced by other nucleophiles, therefore, carbonyl compounds can not undergo nucleophilic substitution reactions.

Only aldehydes, methyl ketones and cyclic ketones react wilh sodium bisulphite.explain why?


Due to the larger size at sulphite ion, it can attack only those carbonyl compounds. where, there is lesser sterie hinderance, that's  why, it reacts with only aldehydes, methyl ketones and cyclic ketones.

Why does benzene undergoes substitution reaction instead of addition reaction?


Benzene nucleus present in all the aromatic hydrocarbons is very stable; it gives a number of substitution reactions but resists addition reactions. Benzene also fails to give tests for unsaturation i.e. it does not decolourise alkaline KMnO4 and bromine water.    
Benzene gives electrophilic substitution due to It is due to the following reasons:    
(2) Due to the presence of π-electron cloud above and below the plane of carbon atoms of the benzene ring.
(2) Benzene ring acts as a source of electrons for electrophilic reagents.  
(3) In electrophilic substitution aromatic character of benzene ring is preserved due to resonance stabilisation. The formation of formation of addition product will destroyed the aromatic ring structure of benzene and therefore addition takes place with very difficulty. On the above explanation we can say that electrophilic substitution reactions are feature of benzene ring.