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

Advertisements
Solution

APPEARS IN
RELATED QUESTIONS
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.
\[\begin{array}{cc}
\ce{CH3 - CH - CH = CH2 + HBr ->[peroxide]}\\
|\phantom{........................}\\
\ce{CH3\phantom{.....................}}
\end{array}\]
Give reason:
Alkyl halides are generally not prepared by free radical halogenation of alkanes.
Convert the following:
But-1-ene to n-butyl iodide
Aromatic electrophilic substitution with iodine can be carried out using _____________
Give reason. Though alkyl halides are moderately polar, they are insoluble in water.
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 pairs of aryl halides cannot be prepared directly by electrophilic substitution?
The compound formed when 3, 5-dinitrobenzoic acid reacts with thionyl chloride is ___________.
Which among the following methods is not suitable for the preparation of alkyl chlorides?
Alkyl halides can be hydrolysed to alcohols by reacting with ____________.
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 ______.
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:
Which one of the following is Swartz reaction?
Explain the preparation of alkyl halide using thionyl chloride (SOCl2).
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}
\end{array}\]
The given compound

is an example of ______.
Which of the following acid strengths is used to get a good yield of alkyl iodide from alcohol and sodium iodide in phosphoric acid?
