Interpretation:
Four isomeric monocarboxylic acids that have five carbon atoms and saturated carbon chain has to be given with their IUPAC names.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula.
For naming a
IUPAC rules for naming a carboxylic acid:
- The longest parent carbon chain is identified that includes the carboxyl group.
- The parent chain name is changed by replacing the suffix “-e” with “-oic acid”.
- Numbering is done in a way that the carboxyl group is designated as number 1. This is not indicated in the part of the name because for carboxylic acid, the carboxyl carbon is always numbered 1.
- The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
- If the carboxyl
functional group is attached to a ring of carbon atoms, the ring is named and “-carboxylic acid” is added as suffix.
Want to see the full answer?
Check out a sample textbook solutionChapter 16 Solutions
GENERAL,ORGANIC,+BIO.CHEM.-MINDTAP
- Write the systematic (IUPAC) names of the given carboxylic acids. CI II H3CCHCH2 -C-OH IUPAC name: II C-OH IUPAC name:arrow_forwardDraw the structure for the carboxylic acid formed by the mild oxidation of 2-propanone.arrow_forwardWrite the structure of the carboxylic acid that forms when the following aldehyde is oxidized: H3C CHarrow_forward
- The chemical reaction where a carboxylic acid reacts with an alcohol in the presence of an inorganic acid source, is called esterification. True Falsearrow_forwardTrue or false The carboxyl group has the same properties as alcohols and aldehydes. Carboxylic acids have lesser hydrogen bonds relative to aldehydes. Carboxylic acids are carbonyl compounds.arrow_forwardGive the structural formula (condensed or skeletal) of the given IUPAC names of saturated hydrocarbons. 1) 2-hydroxybut-3-ynenitrile 2) 1-mercaptohex-5-yne-1,3,3-triol 3) 3-amino-N,N-diethylpentanamide 4) 3-hydroxy-2-oxopropanalarrow_forward
- Draw the structural formula for each of the following and give the classification 10, 20, 30. Draw any oxidation products resulting from a reaction with chromic acid. cyclopropanol 1-methylcyclobutanol 2-methyl-1-hexanol 1-methylcyclohexanol 3-methylcyclohexanol 2,2-dimethylcyclohexanolarrow_forwardExplain the process of Naming Carboxylic Acid Derivatives ?arrow_forwardList the following compounds in order of increasing water solubility: a.ethoxyethane b.propanoic acid c.pentane d.1 butanolarrow_forward
- Give an acceptable alternate name for each of the following branched-chain alkyl groups. a. Isopropyl group b. tert-Butyl group c. (1-Methylpropyl) group d. (2-Methylpropyl) grouparrow_forwardWhat is the functional isomer of butanal? butanoic acid 1-butanol butanone methyl propanoate Other:arrow_forwardWrite the IUPAC names of the given carboxylic acids. CI O H3CCHCH₂-C-OH IUPAC name: HO-C-CH2₂-C-OH IUPAC name:arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning