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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.
\[\ce{CH3 - CH2Br + SbF3 ->}\]
Write the structure and IUPAC name of the major product in the following reaction.
\[\begin{array}{cc}
\ce{CH3 - CH - CH = CH2 + HBr ->[peroxide]}\\
|\phantom{........................}\\
\ce{CH3\phantom{.....................}}
\end{array}\]
Write the structure and IUPAC name of the major product in the following reaction.
Convert the following:
But-1-ene to n-butyl iodide
Which among the following methods is not suitable for the preparation of alkyl chlorides?
Alkyl fluorides are prepared by heating alkyl bromides or chlorides in the presence of metallic fluorides. The reaction is known as ____________ reaction.
Amongst the following, HBr reacts fastest with
Which of the following alkyl halides has the lowest boiling point?
The following reaction is known as:
\[\ce{R - Cl + NaI ->[acetone] R - I + NaCl ↓}\]
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 ______.
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.
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.
Explain Swartz reaction.
How is alkyl halide converted into alcohol by using?
Aqueous NaOH (or KOH)
Explain the preparation of alkyl halide using thionyl chloride (SOCl2).
What is the advantage of alkyl halide using the thionyl chloride (SOCl2 ) method?
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}
\end{array}\]
