Write mechanisms (using curved arrows) for the reaction (deprotonation of an alcohol by a base) for compound 1 converting to compound 2 as outlined in Scheme 1Write mechanisms (using curved arrows) for the reaction (deprotonation of an alcohol by a base) for compound 2 converting to compound 3 as outlined in Scheme 1Write mechanisms (using curved arrows) for the reaction (acid catalysed cleavage of epoxide) for compound 4 converting to compound 5 as outlined in Scheme 1In going from compound 1-4 in Scheme1, why does the OH- attacks that particular ring and carbon as opposed to the double bonds in the other rings or other carbons in the center ring. Need to bear in mind that charged molecules are unstable and nature favors neuralization of charges.