
(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
- (10 pts) The density of metallic copper is 8.92 g cm³. The structure of this metal is cubic close-packed. What is the atomic radius of copper in copper metal?arrow_forwardPredict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2).arrow_forwardPredict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2).arrow_forward
- Q3: Rank the following compounds in increasing reactivity of E1 and E2 eliminations, respectively. Br ca. go do A CI CI B C CI Darrow_forwardQ5: Predict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2). H₂O דיי "Br KN3 CH3CH2OH NaNH2 NH3 Page 3 of 6 Chem 0310 Organic Chemistry 1 HW Problem Sets CI Br excess NaOCH 3 CH3OH Br KOC(CH3)3 DuckDuckGarrow_forwardQ4: Circle the substrate that gives a single alkene product in a E2 elimination. CI CI Br Brarrow_forward
- Please calculate the chemical shift of each protonsarrow_forwardQ1: Answer the questions for the reaction below: ..!! Br OH a) Predict the product(s) of the reaction. b) Is the substrate optically active? Are the product(s) optically active as a mix? c) Draw the curved arrow mechanism for the reaction. d) What happens to the SN1 reaction rate in each of these instances: 1. Change the substrate to Br 'CI 2. Change the substrate to 3. Change the solvent from 100% CH3CH2OH to 10% CH3CH2OH + 90% DMF 4. Increase the substrate concentration by 3-fold.arrow_forwardQ6: Provide the reagents and conditions for the following reactions to make the product with a good yield. Br Br CI она CIarrow_forward
- Q2: We would not expect the following primary alkyl halide to go through an SN1 reaction. However, it can go through an SN1 mechanism. Explain why. Hint: Think about what happens when the leaving group leaves. CI NaO EtOH H བྱིས་ Harrow_forwardI performed this experiment, but I'm so confused. How do I find the first two blank columns using the data provided. What is the [I^-] mol/L and [S2O8^-2] mol/L. How do I find this? Please help!arrow_forwardExample 3 A molecule is achiral if it has a plane of symmetry in any conformation. The given conformation of 2,3-dibromobutane below does not have a plane of symmetry. Will rotation around the C2-C3 bond form a conformation with a plane of symmetry? Draw the conformation to find out. DIY: Do the same for: H3C Brill rotate H CH3 OH HO Brarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningEBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT

