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Williamson's ether reactions imply that an alkoxide reacts with a primary haloalkane. Alkoxides consisting of the conjugate base of an alcohol and are formed by a group R attached to an oxygen atom. They are often written as RO–, where R is the organic substituent (Step 1).
Sn2 reactions are characterized by the reversal of stereochemistry at the site of the leaving group. Williamson's synthesis is no exception and the reaction is initiated by the subsequent attack of the nucleophile. This requires that the nucleophile and electrophile be in anti-configuration (Step 2).
As an example (figure 3).
In the attached file are each of the steps of Williamson's synthesis.
Explanation:
Answer:
Its be 1,2 and 4.
Explanation:
Since changing the direction won't do anything to a electric magnet.
They occur between polar molecules
