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प्रश्न
Write the major products(s) in the following:
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उत्तर
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संबंधित प्रश्न
Which would undergo SN1 reaction faster in the following pair and why?
Given reasons: SN1 reactions are accompanied by racemization in optically active alkyl halides.
AgCN reacts with haloalkanes to form isocyanide. Haloalkanes react with KCN to form alkyl cyanides as the main product. Why?
Arrange the following organic compounds in descending order of their reactivity towards SN1 reaction.
C6H5CH2Br, C6H5CH(C6H5)Br, C6H5CH(CH3)Br, C6H5C(CH3)(C6H5)Br
Which of the following is an example of SN2 reaction?
Which of the following pairs is/are correctly matched?
| Reaction | Product | |
| I | RX + AgCN | RNC |
| II | RX + KCN | RCN |
| III | RX + KNO2 | \[\begin{array}{cc} \phantom{.......}\ce{O}\\ \phantom{.....}/\\ \ce{R - N}\phantom{....}\\ \phantom{.....}\backslash\backslash\\ \phantom{.......}\ce{O} \end{array}\] |
| IV | RX + AgNO2 | \[\ce{R-O-N=O}\] |
Which of the following is the correct order of decreasing SN2 reactivity?
The process of separation of a racemic modification into d and l-enantiomers is called ____________.
Complete the reaction with the main product formed:
Discuss SN2 mechanism of methyl bromide using aqueous KOH.
