Advertisements
Advertisements
प्रश्न
How the following conversion can be carried out?
2-Methyl-1-propene to 2-chloro-2-methylpropane
Advertisements
उत्तर
\[\begin{array}{cc}
\phantom{...}\ce{CH3}\phantom{............................................}\ce{CH3}\phantom{}\\
|\phantom{..................................................}|\\
\ce{\underset{2-Methyl-1-propene}{CH3 - C = CH2} ->[HCl][Markovnikov's rule] H3C - C - CH3}\\
\phantom{...................................................}|\\
\phantom{....................................................}\ce{\underset{2-chloro-2-methylpropane}{Cl}}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Why is sulphuric acid not used during the reaction of alcohols with KI?
Draw the structure of the major monohalo product in the following reaction:
\[\ce{CH3CH2Br + NaI ->}\]
Write the equation for the preparation of 1-iodobutane from 1-butanol.
How will you bring about the following conversion?
Propene to 1-nitropropane
How will you bring about the following conversion?
Ethanol to ethyl fluoride
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH2CH2Cl + NaI ->[acetone][heat]}\]
How the following conversion can be carried out?
Benzyl alcohol to 2-phenylethanoic acid
How the following conversion can be carried out?
tert-Butyl bromide to isobutyl bromide
Among the isomeric alkanes of molecular formula C5H12, identify the one that on photochemical chlorination yields three isomeric monochlorides.
Which is the incorrect option?
3-Methyl-pent-2-ene of peroxide forms an addition product. The number of possible stereoisomers for the product is ______.
Alkyl halides are prepared from alcohols by treating with ______.
Which of the following alcohols will yield the corresponding alkyl chloride on reaction with concentrated HCl at room temperature?
Predict the major product ‘P’ in the following sequence of reactions:
How many products (including stereoisomers) are expected from the monochlorination of the following compound?
\[\begin{array}{cc}
\ce{H3C}\phantom{..................................}\\
\backslash\phantom{...........................}\\
\ce{CH - CH2 - CH3}\\
/\phantom{...........................}\\
\ce{H3C}\phantom{...................................}
\end{array}\]
