Williamson's synthesis involves an SN2 reaction mechanism and is widely used for asymmetric ether synthesis.
Step 1: Williamson's synthesis is used for the preparation of ethers.
Step 2: Reaction: \[ R-O^- + R'-X \rightarrow R-O-R' + X^- \] where \( R'X \) is an alkyl halide and \( R-O^- \) is an alkoxide ion.
Step 3: Example: \[ C_2H_5ONa + CH_3I \rightarrow C_2H_5OCH_3 + NaI \]
Match the amino acid given in List-I with their one-letter code given in List-II
\[ \begin{array}{|l|l|} \hline \textbf{Name of amino acid} & \textbf{One-letter code} \\ \hline (A) \; \text{Lysine} & (I) \; W \\ \hline (B) \; \text{Tryptophan} & (II) \; Q \\ \hline (C) \; \text{Tyrosine} & (III) \; K \\ \hline (D) \; \text{Glutamine} & (IV) \; Y \\ \hline \end{array} \]
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