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प्रश्न
Give reason:
Alkyl halides are generally not prepared by free radical halogenation of alkanes.
उत्तर
Free radical halogenation of alkanes leads to the formation of a mixture of mono and poly halogen compounds. Hence, free radical halogenation of alkanes is not suitable for the preparation of alkyl halides.
संबंधित प्रश्न
Write the structure and IUPAC name of the major product in the following reaction.
\[\begin{array}{cc}
\ce{CH3 - CH - CH2Cl + NaI ->[Acetone]}\\
|\phantom{..................}\\
\ce{CH3\phantom{...............}}
\end{array}\]
Write the structure and IUPAC name of the major product in the following reaction.
\[\ce{CH3 - CH2Br + SbF3 ->}\]
Write the structure and IUPAC name of the major product in the following reaction.
Convert the following:
But-1-ene to n-butyl iodide
The compound formed when 3, 5-dinitrobenzoic acid reacts with thionyl chloride is ___________.
Alkyl fluorides are prepared by heating alkyl bromides or chlorides in the presence of metallic fluorides. The reaction is known as ____________ reaction.
Conversion of an alcohol into alkyl chloride by reacting with thionyl chloride is done in a medium of ____________.
Amongst the following, HBr reacts fastest with
Which of the following alkyl halides has the lowest boiling point?
The following reaction is known as:
\[\ce{R - Cl + NaI ->[acetone] R - I + NaCl ↓}\]
The reaction \[\ce{2R - Cl + COF2 -> 2R - F + COCl2}\] is an example of ______.
What is molecular formula of allyl chloride?
An alkyl iodide on refluxing with aqueous KOH solution gave isopropyl alcohol. The structure of alkyl iodide could be:
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Alkyl chloride when treated with sodium iodide in presence of dry acetone forms alkyl iodide. What is the name of this reaction?
Which one of the following is Swartz reaction?
Choose the false statement from the following.
Explain Swartz reaction.
How is alkyl halide converted into alcohol by using Moist silver oxide?
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}
\end{array}\]
