What nucleophile could be used to react with butyl iodide to prepare the following compound?

The concept is to draw the nucleophile used to prepare an ether (1-ethoxybutane) by reacting with butyl iodide.
Electron rich species are called as nucleophiles and they react with electrophiles. The mechanism of this reaction occurs through an
pathway. This reaction is called Williamson ether synthesis.

Synthesis:

Thus, the nucleophile is,

What nucleophile could be used to react with butyl iodide to prepare the following compound?
What nucleophile could be used to react with butyl iodide to
prepare the following compound?
What nucleophile could be used to react with butyl iodide to prepare the following compound?
What nucleophile could be used to react with butyl iodide to prepare the following compound? Nucleophile + butyl iodide →
What nucleophile could be used to react with butyl iodide to prepare the following compound? + butyl iodide rightarrow
What nucleophile could be used to react with butyl iodide to
prepare the following compound?
1. Unsymmetrical ethers can be made by
the Williamson synthesis, in which an alkoxide ion reacts with an
alkyl bromide. Draw the structure of the alkoxide and the alkyl
bromide needed to produce 2-ethoxy-2-methylpropane (a.k.a t-butyl
ethyl ether), shown below. Show charges where appropriate.
2. What nucleophile could be used to
react with butyl iodide to prepare the following compound?
Explain why the following reaction is not feasible as a synthesis of butyl iodide. It w OH HO + HO-
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