Explain why,
Grignard reagents should be prepared under anhydrous conditions?
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Grignard reagents are very reactive. In the presence of moisture, they react to give alkanes.
$\stackrel{\delta-}{\hbox{R}}\ \stackrel{\delta+}{\hbox{Mg}}\ \stackrel{\delta-}{\hbox{X}}+\text{H}_2\text{O}\rightarrow\text{R}-\text{H}+\text{Mg(OH)X}\\ \text{Grigrard reagent}\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{Alkane}$
Therefore, Grignard reagents should be prepared under anhydrous conditions.
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Write the structure of the major organic product in each of the following reaction:
$\text{C}_6\text{H}_5\text{ONa}+\text{C}_2\text{H}_5\text{Cl}\xrightarrow{}$
Name the following halides according to $\text{IUPAC}$ system and classify them as alkyl, allyl, benzyl $($primary, secondary, tertiary$),$ vinyl or aryl halides: $\ce{CH_3CH_2CH(CH_3)CH(C_2H_5)Cl}.$