HARD
Earn 100

Using Grignard reagent, suggest synthesis of following alcohol from aldehyde or ketone. Whenever possible, suggest more than one combination.

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Important Questions on Alcohols, Phenols, and Ethers

MEDIUM
In the hydroboration - oxidation reaction of propene with diborane, H2O2 and NaOH, the organic compound formed is:
MEDIUM

The aldehydes which will not form Grignard product with one equivalent of Grignard reagents are
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EASY
Propene when treated with cold conc. H2SO4 forms a compound which on heating with water gives
HARD
Give the mechanism for the formation of ethanol from ethene.
MEDIUM
The major product of the following reaction is:
CH3CH=CHCO2CH3LiAlH4
EASY
Upon reaction with CH3MgBr followed by protonation, the compound that produces ethanol is
MEDIUM

The product R of the following reaction sequence is

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EASY
Carry out the following conversions : 
Propene to propanol
EASY
What happens when Propanone is treated with methylmagnesium iodide and then hydrolysed,
EASY
Isobutylene on hydroboration followed by oxidation with hydrogen peroxide in presence of base yields
MEDIUM
What is meant by hydroboration-oxidation reaction? Illustrate it with an example.
HARD

Consider the following sequence of reactions.

 ZPCl5XAlc.KOHY2H2O/ΔConc.H2SO4Z

'Z' is

EASY
A reaction between a carbonyl compound and a Grignard reagent is termed as
MEDIUM
The number of alkene (s) which can produce 2- butanol by the successive treatment of
(i) B2H6 in tetrahydrofuran solvent and
(ii) alkaline H2O2 solution is
EASY

Write the structures of the main products in the following reactions:

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EASY

In the following reaction sequence: 

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Compound I is