(a) Give the mechanism for the formation of ethanol from ethene. (b) Predict the reagent for carrying out the following conversions : (i) Phenol to benzoquinone (ii) Anisole to p-bromoanisole (iii) Phenol to 2,4,6-tribromophenol
(a) Mechanism for the formation of ethanol from ethene-
(b) Reagent for carrying out the following conversions :
(i) Phenol to benzoquinone
(ii) Anisole to p-bromoanisole
(iii) Phenol to 2,4,6-tribromophenol
Out of the following transition elements, the maximum number of oxidation states are shown by
Option: 1 Sc (Z = 21)
Option: 2 Cr (Z = 24)
Option: 3 Mn (Z = 25)
Option: 4 Fe (Z = 26)
The maximum number of oxidation states are shown by Mn.
Hence option C is correct
View Full Answer(1)Iodoform test is not given by
Option: 1 Ethanol
Option: 2 Ethanal
Option: 3 Pentan-2-one
Option: 4 Pentan-3-one
Iodoform test is not given by Pentan-3-one
View Full Answer(1)Give the structures of final products expected from the following reactions :
(i) Hydroboration of propene followed by oxidation with in alkaline medium.
(ii) Dehydration of by heating it with at ..
(iii) Heating of with .
Structures of final products expected from the following reactions :
(i) Hydroboration of propene followed by oxidation with in alkaline medium forms CH3CH2CH2OH
(ii) Dehydration of by heating it with at forms (CH3)2C=CH2
(iii) Heating of with forms
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How can you convert the following ?
(i) Phenol to hydroxybenzaldehyde.
(ii) Methanal to ethanol
(iii) Phenol to phenyl ethanoate.
(i) Phenol to hydroxybenzaldehyde.
(ii) Methanal to ethanol
(iii) Phenol to phenyl ethanoate.
View Full Answer(1)Write the reactions showing the presence of following in the open structure of glucose :
(i) an aldehyde group
(ii) a primary alcohol
(i) an aldehyde group
(ii) a primary alcohol
On oxidation with Nitric acid (HNO3),glucose as well as gluconic acid both yeild a dicarboxylic acid (saccharic acid). This indicates the presence of a primary alcoholic group in glucose.
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(a) Write the mechanism of the following reaction :
(b) Write the equation for the preparation of by Williamson synthesis.
(a)
(b)
View Full Answer(1)How can you convert the following :
(i) Sodium phenoxide to o-hydroxybenzoic acid
(ii) Acetone to propene
(iii) Phenol to chlorobenzene
(i) Sodium phenoxide to o-hydroxybenzoic acid
(ii) Acetone to propene
(iii) Phenol to chlorobenzene
View Full Answer(1)(a) Write the mechanism of the following reaction :
(b) Write the preparation of phenol from cumene.
(a)
(b) Preparation of phenol from cumene
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