The structure of cyclopentane-1,2-diol
1 answer:
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Answer:1-methoxy-2,4-dinitrobenzene
Explanation:
The nitro groups are strongly electron withdrawing and promote nucleophilic substitution reactions where one of the original substituents is removed and replaced by a strong nucleophile such as the methoxy group. The mechanism of the reaction is attached below. The electron withdrawing nitrogroup assists the formation of the intermediate in the reaction as shown.
Answer:
b . 0.351 L.
Explanation:
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In this case, since diluted solutions are prepared by adding an extra amount of diluent to a stock-concentrated solution, we infer that the number of moles of solute remains the same, therefore we can write:
Thus, solving for the volume of the stock solution, V1, we obtain:
Now, by plugging in the given data we obtain:
Therefore, the answer is b . 0.351 L.
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