(a)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: Aldol condensation is defined as a condensation reaction that involves the nucleophilic addition of an enolate ion to another carbonyl group to form a
(b)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: In the claisen-ester condensation, nucleophilic acyl substitution takes place on an ester. The enolate ion acts as a nucleophile. It attacks the carbonyl carbon to form a tetrahedral intermediate. Acidity of beta-keto ester products is higher than simple ketones, aldehydes and esters.
(c)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: Intramolecular aldol reactions of diketones are used for the formation of five and six membered rings. These reactions are known as aldol cyclizations. Aldol cyclization of rings which are larger than six and smaller than five is less common.
(d)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: Condensation reaction that takes place between two carbonyl group containing molecules involves both nucleophilic addition and alpha substitution. Such a condensation reaction is known as carbonyl condensation reaction. One carbonyl is converted into a nucleophilic enolate ion by a base in this reaction.
(e)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: Condensation reaction that takes place between two carbonyl group containing molecules involves both nucleophilic addition and alpha substitution. Such a condensation reaction is known as carbonyl condensation reaction. One carbonyl is converted into a nucleophilic enolate ion by a base in this reaction.
(f)
To determine: The synthesis of the given compound with the help of an aldol, claisen or another type of condensation.
Interpretation: The given compound with the help of an aldol, claisen or another type of condensation is to be synthesized.
Concept introduction: Condensation reaction that takes place between two carbonyl group containing molecules involves both nucleophilic addition and alpha substitution. Such a condensation reaction is known as carbonyl condensation reaction. One carbonyl is converted into a nucleophilic enolate ion by a base in this reaction.

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Chapter 22 Solutions
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
- The Ka for sodium dihydrogen phosphate is 6.32 x 10-8. Find the pH of a buffer made from 0.15 M H2PO4- and 0.25 M HPO42- .arrow_forwardThe Ka for lactic acid is 1.4 x 10-4. Find the pH of a buffer made from 0.066 M lactic acid and 0.088 M sodium lactate.arrow_forwardZaitsev's Rule 3) (a) Rank the following alkenes in order of decreasing stability. most stable A B C D > > > (b) Rank the following carbocations in order of decreasing stability least stable B C Darrow_forward
- Calculate the percent ionization for 0.35 M nitrous acid. Use the assumption to find [H3O+] first. K = 7.1 x 10-4arrow_forwardFor each of the following reactions: Fill in the missing reactant, reagent, or product (s), indicating stereochemistry where appropriate using dashed and wedged bonds. If the reaction forms a racemic mixture, draw both structures in the box and write the word “racemic”.arrow_forward5) Using the carbon-containing starting material(s), propose a synthesis based on the following retrosynthetic analysis. Provide structures for all intermediates. The carbon atoms in the product must originate from the starting material(s), but you may use as many equivalents of each starting material as you would like, and any reagent/reaction you know (note: no mechanisms are required). H H =arrow_forward
- Calculate the percent ionization for 0.0025 M phenol. Use the assumption to find [H3O+] first. K = 1.0 x 10-10arrow_forward10:04 AM Tue Mar 25 Sunday 9:30 AM 95% Edit Draw the corresponding structures in each of the boxes below: Ester Name Methyl butyrate (Example) Alcohol Structure H3C-OH Acid Structure Ester Structure Isoamyl acetate Ethyl butyrate Propyl acetate Methyl salicylate Octyl acetate Isobutyl propionate Benzyl butyrate Benzyl acetate Ethyl acetate H₂C OH HCarrow_forward2) For each of the following reactions: (i) (ii) Fill in the missing reactant, reagent, or product (s), indicating stereochemistry where appropriate using dashed and wedged bonds. If the reaction forms a racemic mixture, draw both structures in the box and write the word "racemic". (a) (b) 1) R₂BH 2) H₂O2, NaOH (aq) HBr Br racemic Br + Br Br racemicarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningEBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT

