Concept explainers
(1)
Interpretation:
The most acidic hydrogens in the given compounds are to be indicated.
Concept introduction:
The substances that produce hydrogen ions (
According to the definition of Bronsted and Lowry, acids are the substances that donate protons whereas bases are the substances that accept protons.
(1)
Answer to Problem 22.60SP
The most acidic hydrogens in the given compounds are shown in Figure 1.
Explanation of Solution
In a molecule, different types of protons are present. However, when acting as acids, only the most acidic proton participates in the acid-base reaction. The protons of
Acidic hydrogen is defined as that hydrogen which is attached to more electronegative atoms like oxygen and fluorine. The compound (f) does not contain any acidic hydrogen atom in the given compounds.
The most acidic hydrogens in the given compounds are shown below.
Figure 1
(2)
Interpretation:
The structures of important resonance contributors of the anions of the given compounds are to be drawn.
Concept introduction:
The delocalization of electrons due to presence of lone pair and double bond is called resonating structure. The structure is more stable if the resonating structures are more.
(2)
Answer to Problem 22.60SP
The structures of important resonance contributors of the anions of the given compounds are shown below.
Explanation of Solution
The formation of carbanion occurs when acidic hydrogen is removed from a compound. The important resonance contributors of the anions that results from the removal of most acidic hydrogen are shown below.
(a)
Figure 2
(b)
Figure 3
(c)
Figure 4
(d)
Figure 5
(e)
Figure 6
(f)
The given compound is shown below.
Figure 7
The given compound does not contain any acidic hydrogen atom. Therefore, it does not show resonance structures.
(g)
Figure 8
(h)
Figure 9
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Chapter 22 Solutions
ORGANIC CHEMISTRY
- Please 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_forwardThe plutonium isotope with 144 neutrons Enter the chemical symbol of the isotope.arrow_forward
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- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning