Concept explainers
(a)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of
Answer to Problem 42P
Explanation of Solution
The reaction of C6 H5 -CH2 -COOH with sodium carbonate forms sodium salt of C6 H5 -CH2 -COOH with water and carbon dioxide gas.
(b)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
Explanation of Solution
The reaction of C6 H5 -CH2 -COOH with sodium hydroxide forms sodium salt of C6 H5 -CH2 -COOH with water. This is a neutralization reaction as carboxylic acid reacts with base to form salt.
(c)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
Explanation of Solution
The reaction of C6 H5 -CH2 -COOH with ammonia solution forms ammonium salt of C6 H5 -CH2 -COOH that is ammonium phenyl acetate.
(d)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
Explanation of Solution
The reaction of C6 H5 -CH2 -COOH with lithium ammonium hydride followed by hydrolysis leads to formation of 2-phenylethanol. This is an example of reduction reaction and LiAlH4 is a reducing agent.
(e)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
C6 H5 -CH2 -COOH + NaBH4 / H2 O (No reaction.
Explanation of Solution
NaBH4 with water is a weak reducing agent therefore it cannot reduce the carboxylic acid and no reaction is observed with it.
(f)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
Explanation of Solution
Reaction of phenyl acetic acid with methanol in acidic medium as catalyst forms ester with water. This reaction is called as Fisher Esterification reaction.
(g)
Interpretation:
The reaction of phenyl acetic acid with given reagents should be completed.
Concept Introduction:
Phenylacetic acid contains one −COOH group with molecular formula C6 H5 -CH2 -COOH. Carboxylic acids react with base to form salt and water. This reaction is called as neutralization reaction. The reduction of carboxylic acid form carbonyl compounds and alcohols whereas reaction with alcohol forms ester.
Answer to Problem 42P
Explanation of Solution
H2 / Ni cannot reduce carboxylic acid group as it is reducing agent for
Want to see more full solutions like this?
Chapter 17 Solutions
Introduction to General, Organic and Biochemistry
- 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. 4arrow_forwardc. Serricornin, the female-produced sex pheromone of the cigarette beetle, has the following structure. OH What is the maximum number of possible stereoisomers? Is this structure a meso compound? d. Please consider the natural product alkaloids shown below. Are these two structures enantiomers, diastereomers or conformers? H HO H H HN HO HN R R с R=H cinchonidine R=ET cinchonine Harrow_forwardNail polish remover containing acetone was spilled in a room 5.23 m × 3.28 m × 2.76 m. Measurements indicated that 2,250 mg of acetone evaporated. Calculate the acetone concentration in micrograms per cubic meter.arrow_forward
- Please help me answer number 1. 1. If your graphs revealed a mathematical relationship between specific heat and atomic mass, write down an equation for the relationship. I also don't understand, is the equation from the line regression the one that I'm suppose use to show the relationship? If so could you work it all the way out?arrow_forwardDescribe the principle of resonance and give a set of Lewis Structures to illustrate your explanation.arrow_forwardDon't used hand raitingarrow_forward
- It is not unexpected that the methoxyl substituent on a cyclohexane ring prefers to adopt the equatorial conformation. OMe H A G₂ = +0.6 kcal/mol OMe What is unexpected is that the closely related 2-methoxytetrahydropyran prefers the axial conformation: H H OMe OMe A Gp=-0.6 kcal/mol Methoxy: CH3O group Please be specific and clearly write the reason why this is observed. This effect that provides stabilization of the axial OCH 3 group in this molecule is called the anomeric effect. [Recall in the way of example, the staggered conformer of ethane is more stable than eclipsed owing to bonding MO interacting with anti-bonding MO...]arrow_forward206 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_forward
- 5. 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_forwardThe mass ratio of sodium to fluorine in sodium fluoride is 1.21:1. A sample of sodium fluoride produced 26.1 gg of sodium upon decomposition. How much fluorine was formed?arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning