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प्रश्न
Write the structure of an isomer of compound C4H9Br which is most reactive towards SN1 reaction
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उत्तर
It is the most reactive towards the SN1 reaction.
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संबंधित प्रश्न
In the following pair of halogen compounds, which compound undergoes a faster SN1 reaction?
How will you bring about the following conversion?
Toluene to benzyl alcohol
Write the structure of the major organic product in the following reaction:
\[\ce{CH3CH(Br)CH2CH3 + NaOH ->[water]}\]
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 | \[\ce{R-O-N=O}\] |
An important chemical method to resolve a racemic mixture makes use of the formation of ______.
Which of the following alkyl halides will undergo SN1 reaction most readily?
A primary alkyl halide would prefer to undergo ______.
Compound ‘A’ with molecular formula \[\ce{C4H9Br}\] is treated with aq. \[\ce{KOH}\] solution. The rate of this reaction depends upon the concentration of the compound ‘A’ only. When another optically active isomer ‘B’ of this compound was treated with aq. \[\ce{KOH}\] solution, the rate of reaction was found to be dependent on concentration of compound and \[\ce{KOH}\] both.
(i) Write down the structural formula of both compounds ‘A’ and ‘B’.
(ii) Out of these two compounds, which one will be converted to the product with inverted configuration.
Racemisation occurs in ______.
Complete the reaction with the main product formed:
