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Question
Write the structure of the major organic product in the following reaction:
\[\ce{C6H5ONa + C2H5Cl ->}\]
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Solution 1
\[\ce{\underset{sodium phenoxide}{C6H5O^-Na} + \underset{ethyl chloride}{C2H5Cl} ->[Williamson Synthesis] \underset{phenetole}{C_6H_5 - O - C_2H_5} + NaCl}\]
Solution 2
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\[\begin{array}{cc}
\ce{Br}\phantom{......}\\
|\phantom{.......}\\
\ce{CH3-CH2-CH-CH2-CH-CH3}\\
\phantom{...............}|\\
\phantom{................}\ce{Br}
\end{array}\]
with excess Mg/Et2O(Et = C2H5) is:
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Explain why Grignard reagents should be prepared under anhydrous conditions?
Explain why Grignard reagents should be prepared under anhydrous conditions?
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Explain why Grignard reagents should be prepared under anhydrous conditions?
