Advertisements
Advertisements
Question
Give reason:
Alkyl halides are generally not prepared by free radical halogenation of alkanes.
Advertisements
Solution
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.
RELATED QUESTIONS
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.

Write the structure and IUPAC name of the major product in the following reaction.

What is Grignard reagent? How is it prepared? Why are they prepared under anhydrous condition?
Predict all the alkenes that would be formed by dehydrohalogenation of the following alkyl halide.
- 2-chloro-2-methylbutane
- 3-bromo-2,2,3-trimethylpentane
Which of the following reaction proves the chlorinating property of phosphorus pentachloride?
Which of the following pairs of aryl halides cannot be prepared directly by electrophilic substitution?
The compound formed when 3, 5-dinitrobenzoic acid reacts with thionyl chloride is ___________.
Identify Sandmeyer's reaction from the following.
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?
Which reaction is useful in exchange of halogen in alkyl chloride by iodide?
Identify the INCORRECT statement.
The following reaction is known as:
\[\ce{R - Cl + NaI ->[acetone] R - I + NaCl ↓}\]
What is the relative rate of SN2 reaction for (CH3)3C - Br?
Identify 'A' in the following reaction: \[\ce{C2H5OH + HCl ->[A] C2H5Cl + H2O}\]
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:
Identify the name of reaction in which alkyl fluorides are prepared by heating alkyl bromide with metallic fluorides.
How is alkyl halide converted into alcohol by using Moist silver oxide?
What is the advantage of alkyl halide using the thionyl chloride (SOCl2 ) method?
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}
\end{array}\]
