(a)
Interpretation:
The number of carbon atoms present in Formic acid has to be given.
Concept Introduction:
In
Common name for monocarboxylic acid is formed by taking Greek or Latin root name for the number of carbon atom that is appended by suffix “ic acid”
(b)
Interpretation:
The number of carbon atoms present in Caproic acid has to be given.
Concept Introduction:
In organic chemistry compounds are given common names also apart from IUPAC names. Common names are derived from the Greek-letter system. This is used in numbering of the carbon atoms in a carbon chain. Common names are also derived from the Greek or Latin word that represents the source of the acid.
Common name for monocarboxylic acid is formed by taking Greek or Latin root name for the number of carbon atom that is appended by suffix “ic acid”
(c)
Interpretation:
The number of carbon atoms present in Succinic acid has to be given.
Concept Introduction:
In organic chemistry compounds are given common names also apart from IUPAC names. Common names are derived from the Greek-letter system. This is used in numbering of the carbon atoms in a carbon chain. Common names are also derived from the Greek or Latin word that represents the source of the acid.
Common name for monocarboxylic acid is formed by taking Greek or Latin root name for the number of carbon atom that is appended by suffix “ic acid”
(d)
Interpretation:
The number of carbon atoms present in Malonic acid has to be given.
Concept Introduction:
In organic chemistry compounds are given common names also apart from IUPAC names. Common names are derived from the Greek-letter system. This is used in numbering of the carbon atoms in a carbon chain. Common names are also derived from the Greek or Latin word that represents the source of the acid.
Common name for monocarboxylic acid is formed by taking Greek or Latin root name for the number of carbon atom that is appended by suffix “ic acid”
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Chapter 16 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- 1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forwardCondensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forward
- What is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forwardWhich representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward
- 3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forwardIn the box below, specify which of the given compounds are very soluble in polar aprotic solvents. You may select more than one compound. Choose one or more: NaCl NH4Cl CH3CH2CH2CH2CH2CN CH3CH2OH hexan-2-one NaOH CH3SCH3arrow_forward
- On the following structure, select all of the atoms that could ACCEPT a hydrogen bond. Ignore possible complications of aromaticity. When selecting be sure to click on the center of the atom.arrow_forwardRank the compounds below from lowest to highest melting point.arrow_forward18 Question (1 point) Draw the line structure form of the given partially condensed structure in the box provided. :ÖH HC HC H2 ΙΩ Н2 CH2 CH3 CH3 partially condensed formarrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
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