What would the mechanism be for number 5 (c)If an alcohol is used instead of water, ethers are produced. Draw a mechanism for the following:OMeMeOH[H,SOJMany reactions are Intramolecular. Here the reactants are both in the same molecule. Draw a mechanism toexplain the following:(H2SO15. Mercury is toxic and used only when necessary for synthesis.mercuration/demercuration scheme could be used to give products of alkene hydration without rearrangementFor each of the following reactions, give the product of each and indicate the product you would obtain by simpIn class we learned that the oxhydration in aqueous acid.DELL

Acid-catalyzed ether formation: Alkene in presence of H+ forms carbonation. The non-bonding electrons (lone pairs) of alcohol(nucleophile) will attack the carbocation and ether is formed as a product. This ether formation can be of two types : 1. Intermolecular ether bond formation: After acid-catalyzed carbonation formation if the upcoming nucleophile comes from the medium then the reaction is called Intermolecular ether bond formation. 2. Intramolecular ether bond formation: After acid-catalyzed carbonation formation if the nucleophile of the same molecule attacks the carbonation and ether bond is formed. Then the reaction is called intramolecular ether bond formation1. Intermolecular ether bond formation: The detailed mechanism is given below :2. Intramolecular ether bond formation: