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प्रश्न
Write the structure and IUPAC name of the major product in the following reaction.
उत्तर
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संबंधित प्रश्न
Write the structure and IUPAC name of the major product in the following reaction.
\[\begin{array}{cc}
\ce{CH3 - CH - CH = CH2 + HBr ->[peroxide]}\\
|\phantom{........................}\\
\ce{CH3\phantom{.....................}}
\end{array}\]
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 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.
Which among the following methods is not suitable for the preparation of alkyl chlorides?
What is the name of reaction involving replacement of diazonium group by chloride using cuprous (I) salt?
Alkyl halides can be hydrolysed to alcohols by reacting with ____________.
Alkyl fluorides are prepared by heating alkyl bromides or chlorides in the presence of metallic fluorides. The reaction is known as ____________ reaction.
Which of the following alkyl halides has the lowest boiling point?
Identify the INCORRECT statement.
What is the relative rate of SN2 reaction for (CH3)3C - Br?
The reaction \[\ce{2R - Cl + COF2 -> 2R - F + COCl2}\] is an example of ______.
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?
The conversion of ethyl bromide using sodium iodide and dry acetone, this reaction is know as ______.
Choose the false statement from the following.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}
\end{array}\]