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प्रश्न
Write the structures of the main products when acetone (CH3 − CO − CH3) reacts with the following reagents :
CH3MgBr and then H3O+
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उत्तर
Acetone reduces to form tertiary alcohol in presence of grignard reagent.
संबंधित प्रश्न
How will you convert: Propene to Propan-2-ol?
How is the following conversion carried out?
\[\ce{Methyl magnesium bromide → 2-Methylpropan-2-ol}\]
Name the reagent used in the following reaction:
Butan-2-one to butan-2-ol.
Write the structure of main compounds A and B in the following reaction:
\[\ce{CH3CH2CN->[CH3MgBRH/3O+]A->[LiAIH4]B}\]
Primary alcohols are prepared by the reduction of carboxylic acids. Though lithium aluminium hydride is a strong reducing agent, it is not used in the reaction. This is so because:
Which of the following reacts with NaOH to give alcohol?
Commercially carboxylic acids are reduced to alcohols by converting them to the ______.
When alcohol react with concentrated H2SO4 intermediate compound formed is
To synthesise 1.0 mole of 2-methylpropan-2-ol from Ethylethanoate ______ equivalents of CH3MgBr reagent will be required. (Integer value)
The products "A" and "B" formed in above reactions are:
