No it is redistributed and the state changes to gas and liquid
<span>The enthalpy of an intermediate step when used to produce an overall chemical equation should be manipulated in this way:
</span><span>Multiply the enthalpy by –1 if the chemical equation is reversed.
If the forward reaction requires energy, the reverse will produce energy.</span>
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.