Advertisements
Advertisements
प्रश्न
Show how you would synthesise the following alcohol from an appropriate alkene?

Advertisements
उत्तर

APPEARS IN
संबंधित प्रश्न
Show how is the following alcohol prepared by the reaction of a suitable Grignard reagent on methanal?
\[\begin{array}{cc}
\ce{CH3 - CH - CH2OH}\\
|\phantom{........}\\
\ce{CH3}\phantom{....}\\
\end{array}\]
How is the following conversion carried out?
\[\ce{Ethyl magnesium chloride -> Propan-1-ol}\]
Name the reagent used in the following reaction:
Dehydration of propan-2-ol to propene.

Show how you would synthesise the following alcohol from an appropriate alkene?

How will you convert: Phenol to 2, 4, 6 − trinitrophenol?
Write the structure of main compounds A and B in the following reaction:
\[\ce{CH3CH2CN->[CH3MgBRH/3O+]A->[LiAIH4]B}\]
Ketones react with Grignard reagent to produce ____________.
Which of the following reacts with NaOH to give alcohol?
Why is the reactivity of all the three classes of alcohols with conc. \[\ce{HCl}\] and \[\ce{ZnCl2}\] (Lucas reagent) different?
The Wittig reaction is a reaction between a carbonyl compound (aldehyde or ketone only) and a species known as a phosphoniumylide. What is the expected final product in the Wittig reaction?
Select the acid(s) which cannot be prepared by Grignard reagent.
The reagent used for dehydration of an alcohol is
The best reagent to convert pent 3 – en 2 – 01 into pent 3 – in – 2 – one is
The major product of acid catalysed dehydration of 1-methylcyclohexanol is ______.
To synthesise 1.0 mole of 2-methylpropan-2-ol from Ethylethanoate ______ equivalents of CH3MgBr reagent will be required. (Integer value)
\[\ce{C3H8O ->[{[O]}][K2Cr2O7/H2SO4] C3H6O ->[I2 + NaOH(aq.)] CHI3}\]
In this reaction the first compound is:
Given below are two statements:
Statement I: On heating with KHSO4, glycerol is dehydrated and acrolein is formed.
Statement II: Acrolein has a fruity odour and can be used to test glycerol's presence.
Choose the correct option.
Write the mechanism of acid dehydration of ethanol to yield ethene.
How are the following conversion carried out?
\[\ce{Methyl magnesium bromide -> 2-Methylpropan-2-ol}\]
