Concept explainers
(a)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
(b)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Reaction with
Reaction with excess dimethylamine:
Acid chloride gets converted into dimethylamide on reaction with excess dimethylamine.
(c)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Reaction with
Amide gets converted into nitrile on reaction with
(d)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Hydrolysis of ester:
Ester is hydrolysed into carboxylic acid in presence of an acid catalyst. This reaction is known as ester hydrolysis.
Acetylation of ester:
Carboxylic acid gets converted into anhydride on reaction with acetyl chloride.
(e)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Reaction with
Ester gets reduced as aldehyde on reaction with
(f)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Acetylation reaction:
Phenol gets converted into acetate on treatment with anhydride.
(g)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Reaction with acid chloride:
(h)
Interpretation: To Predict the major products for the given reactions.
Concept Introduction:
Hydrolysis of cyclic ester:
Reaction of a cyclic ester with the water molecule is known as hydrolysis. When it takes place in the presence of an acid catalyst, then it will be known as acid-catalyzed hydrolysis of the cyclic ester which results in the bifunctional molecule.

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Chapter 20 Solutions
Organic Chemistry
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- What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.arrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density × NO2 ○ donating O donating O withdrawing O withdrawing O electron-rich electron-deficient no inductive effects O no resonance effects O similar to benzene E [ CI O donating withdrawing O no inductive effects Explanation Check ○ donating withdrawing no resonance effects electron-rich electron-deficient O similar to benzene © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardUnderstanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forward
- Identifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forward
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