Q.Write IUPAC names of the following compounds:
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Start your 14-day free trial to unlock the full solution →(i) is a mixed acid anhydride, (ii) is a small-ring carbaldehyde, (iii) is an ether named as an alkoxyalkane, and (iv) is a branched amino-diacid-aldehyde named with carboxylic acid as the principal characteristic group.
(i) CH3-CO-O-CO-CH2CH3: This is an anhydride formed from two different carboxylic acids -- acetic acid (CH3COOH) and propanoic acid (CH3CH2COOH) -- joined through a shared oxygen with loss of water. Mixed anhydrides are named by citing both parent acid names alphabetically, followed by "anhydride": acetic propanoic anhydride (formally, ethanoic propanoic anhydride).
(ii) A small ring bearing a -CHO group: based on the figure description, this is a small skeletal ring (three- or four-membered) with an aldehyde substituent. Taking the most standard reading of such a ring-with-CHO structure at this level, it is cyclopropanecarbaldehyde (cyclopropane-1-carbaldehyde), i.e., a cyclopropane ring with one ring carbon bearing a -CHO group. Note of honesty: the original scan's ring outline was described as ambiguous between a cyclopropane (3-membered) and cyclobutane (4-membered) ring; if the ring is in fact four-membered, the correct name would instead be cyclobutanecarbaldehyde (cyclobutane-1-carbaldehyde) -- the naming pattern (ring name + "carbaldehyde") is identical either way, only the ring-size prefix changes.
(iii) CH3O-C(CH3)3: The central carbon bears three methyl groups and is bonded to an -O-CH3 (methoxy) group. Naming it as an alkoxyalkane, the parent chain is propane (the tert-butyl carbon skeleton, C1-C2-C3, with two extra methyls at C2), with a methyl and a methoxy group both at C2: 2-methoxy-2-methylpropane (common name: tert-butyl methyl ether, MTBE).
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