(a)
Interpretation: The IUPAC name for Megatomoic acid has to be given.
Concept introduction:
Carboxylic acids contain a carbonyl attached to a hydroxyl group as shown below,
Nomenclature of
- Find the Parent hydrocarbon chain.
- Carboxyl carbon must be numbered first.
- Replace the –e in the
alkane name with –oic acid.
Naming of compounds with two
If a compound has two functional groups, the one with lower priority is indicated by a prefix and another with the higher priority by a suffix.
E-Z designators are used as like cis-trans terminology for non-similar groups attached
In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight. If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
(b)
Interpretation: The number of possible stereoisomers for the given compound has to be stated.
Concept introduction:
Carboxylic acids contain a carbonyl attached to a hydroxyl group as shown below,
The stereoisomerism is the arrangement of atoms in molecules whose connectivity remains the same but their arrangement in different in each isomer.
The two molecules are described as stereoisomers if they are made of the same atoms connected in the same sequence, but the atoms are positions differently in space
E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight. If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
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Organic Chemistry
- Compounds that contain an N-H group associate by hydrogen bonding. (a) Do you expect this association to be stronger or weaker than that of compounds containing an O-H group? (b) Based on your answer to part (a), which would you predict to have the higher boiling point, 1-butanol or 1-butanamine?arrow_forwardProvide the IUPAC name for each of the following compounds. (a) (b) H3CO- (c) NH2 OH H,N- CIarrow_forwardGive IUPAC Nomenclature for both compounds.arrow_forward
- Draw one possible structure for each of the following compounds based on the descriptions below. (i) A compound with molecular formula C6H11NO that includes alkene, secondary amine, and primary alcohol functional groups. (ii) A compound with molecular formula C6H9NO that has an amide functional group and does not have an alkene group.arrow_forwardIdentify the class of the compound based on its functional groups. .0. H3C CH3 H3C° H3C H. (a) (b) (c) alcohol alcohol alcohol ether ether ether aldehyde aldehyde aldehyde ketone ketone ketone carboxylic acid carboxylic acid carboxylic acid ester ester ester amine amine amine :0:arrow_forwardDraw the structures of the following compounds. (a)methylene chloridearrow_forward
- Ethanol (CH3CH2OH) and dimethyl ether (CH3OCH3) are constitutional isomers. (a) Predict which of the two has the higher boiling point. (b) Predict which of the two is more soluble in water.arrow_forwardis (b) 2, 3-dimetlyp (c) 2-ethyl-3-methylbutanal (d) 2-ethyl-3-methylbutan-3-al The IUPAC name of is CHO 2. Br (a) 2-methyl-3-bromohexanal (b) 3-bromo-2-methylbutanal (c) 2-methyl-3-bromobutanal (d) 3-bromo-2-methylpentanal 3. The IUPAC name of the compound HO is (a) 2-ethenyl-3-methyl cyclohexa-1, 3-diene (b) 2, 5-dimethyl hepta-2, 6-dienoic acid (c) 2, 6-dimethyl hepta-2, 5-dienoic acid (d) 2, 3-dimethyl epoxyethane 4. The IUPAC name of the compoundarrow_forwardOf the two compounds, which is more soluble in water? (a) CH3CCH3 CH3CH2CI First Second (b) CH3CH2CCH2CH2CH3 First NaCl Secondarrow_forward
- Write condensed formulas and provide IUPAC names for the following compounds:(a) ethyl alcohol (in beverages)(b) methyl alcohol (used as a solvent, for example, in shellac)(c) ethylene glycol (antifreeze)(d) isopropyl alcohol (used in rubbing alcohol)(e) glycerinearrow_forward(a) A phenyl group has the molecular formula CH- and is represented by the symbol Bn. True False (b) Para substituents occupy adjacent carbons on a benzene ring. (c) True False (e) 3-Bromobenzoic acid can be separated into cis and trans isomers. True O False (d) 1-Phenylcyclohexene is a planar molecule. True False Benzene, naphthalene, and phenanthrene are polynuclear aromatic hydrocarbons (PAHs). Truearrow_forward[10] 10] Q1. Do the following conversions as directed. Write the complete reaction equation. (a) Benzaldehyde to Benzoic Acid. (b) Propanal to 1-propanal (c) Cyclohexanone to Cyclohexanol (d) Acetaldehyde to Ethyl alcohol (e) Acetone to Iso-propyl alcoholarrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning