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.
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Wednesday, January 29, 2020
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?
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.
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