(a)
Interpretation:
Aldehyde must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom.
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a
(b)
Interpretation:
Ketone must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
(c)
Interpretation:
Ester must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
(d)
Interpretation:
Carboxylic acid must contain a carbon‑oxygen single bond or not has to be indicated.
Concept Introduction:
Carbonyl groups are the one which contain a double bond between carbon and oxygen atom. Aldehydes and ketones possess this carbonyl functional group in it. The structural representation of a carbonyl group can be given as shown below,
The groups that is attached to the carbonyl carbon atom can be either hydrogen or carbon atom. If the attached atoms are hydrogen and a carbon atom means then the compound is an aldehyde and if they are two carbon atoms means then the compound is a ketone. If the attached atom is a nitrogen atom to the carbonyl carbon atom means it is a amide. If a hydroxyl group is attached to a carbonyl carbon atom, then it is a carboxylic acid. If one of the bonds in the carbonyl carbon atom is attached to an oxygen atom that is bonded with alkyl, cycloalkyl or aromatic system is known as ester.
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Chapter 15 Solutions
General, Organic, And Biological Chemistry, Hybrid (with Owlv2 Quick Prep For General Chemistry Printed Access Card)
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- 206 Pb 82 Express your answers as integers. Enter your answers separated by a comma. ▸ View Available Hint(s) VAΣ ΜΕ ΑΣΦ Np, N₁ = 82,126 Submit Previous Answers ? protons, neutronsarrow_forwardPlease draw the inverted chair forms of the products for the two equilibrium reactions shown below. Circle the equilibrium reaction that would have a AG = 0, i.e., the relative energy of the reactant (to the left of the equilibrium arrows) equals the relative energy of the product? [No requirement to show or do calculations.] CH3 CH3 HH CH3 1 -CH3arrow_forward5. Please consider the Newman projection of tartaric acid drawn below as an eclipsed conformer (1). Please draw the most stable conformer and two intermediate energy conformers noting that staggered conformers are lower in energy than eclipsed forms even if the staggered conformers have gauche relationships between groups. [Draw the substituents H and OH on the front carbons and H, OH and CO₂H on the back carbons based on staggered forms. -CO₂H is larger than -OH.] OH COH ICOOH COOH COOH 1 2 COOH COOH 3 4 Staggered Staggered Staggered (most stable) Indicate the number of each conformer above (1, 2, 3 and 4) that corresponds to the relative energies below. Ref=0 Rotation 6. (60 points) a. Are compounds 1 and 2 below enantiomers, diastereomers or identical? OH OH HO HO LOH HO HO OH 2 OH OH b. Please complete the zig-zag conformation of the compound (3R,4S)-3,4-dichloro-2,5-dimethylhexane by writing the respective atoms in the boxes. 3.arrow_forward
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