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(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 5 Solutions
Organic And Biological Chemistry
- Draw the Fischer projection for a D-aldo-pentose. (aldehyde pentose). How many total stereoisomers are there? Name the sugar you drew. Draw the Fischer projection for a L-keto-hexose. (ketone pentose). How many total stereoisomers are there? Draw the enantiomer.arrow_forwardDraw a structure using wedges and dashes for the following compound: H- Et OH HO- H H- Me OHarrow_forwardWhich of the following molecules are NOT typical carbohydrates? For the molecules that are carbohydrates, label them as an aldose or ketose. HO Он ОН ОН Он ОН но ΤΗ HO ОН HO eve Он он ОН ОН ОН If polyethylene has an average molecular weight of 25,000 g/mol, how many repeat units are present?arrow_forward
- Draw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forwardWhat are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward
- 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
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
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