(C10H12) 1) O3 2) DMS (C,H160) 1) EtMgBr 2) H20 C (C9H100) (CH3)2NH H+ B Dean-Stark AICI3

Q: Explain the reactivity and orientation effects observed in each heterocycle.a. Pyridine is less…

A: Aromatic compounds generally shows electrophilic substitution reactions. In electrophilic…

Q: 21 of 42 Current Attempt in Progress A Propose an efficient synthesis for the given transformation.…

A: DCM Explanation:Step 1: Reaction Mechanism Step 2: Alkyl halide reacts with Mg to form the Grignard…

Q: Br2 NaOH Bra. C 1. LDA (excess) D 1. NaH B H,C CH, hr E 2. CH,Br CI, 2. H,0º

A: when alkane reacts with Br2/hv then it will give Alkyle Bromide as a product, and this reaction is…

Q: Which reagents will give the transformation shown? OH

A: The given reaction is the transformation of alkene to less-substituted alcohol.

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A: Alkyl halides on treatment with NaCN undergo nucleophilic substitution reactions to form cyanides as…

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A: Electron donating group (EDG) on benzene ring increases its reactivity towards electrophilic…

Q: 1. Propose the mechanisms and predict the products of the following reactions. a) b) OH OH H₂SO4…

A: The given reactions are dehydration reactions of alcohol, which lead to the formation of an…

Q: Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or…

A: The given reaction involves three steps, such as,  1. Reductive amination of aldehyde to form amine.…

Q: HCI - 20°С

A: •Here given a  reaction between alkene and HCl at low temperature(-20°C). •Reaction will be:-

Q: Please give appropriate structure for compound A. Compound A has 6 carbons, two stereocenters (both…

A: To identify the Compound A and to propose a reaction scheme using Compound A as the acid and an base…

Q: 3. Design a retrosynthetic and a synthetic scheme for the following compounds: CO2CH3 COCH3 Br b)…

A: RETROSYNTHETIC ANALYSIS Retrosynthetic analysis is described as the method of transforming target…

Q: Which compound in the following pair is more basic? N. I II IZ:

A: Which compound in the following pair is more basic ?

Q: Provide the product and an arrow pushing mechanism for the reaction shown below. MeOK then شد

A: This is an example of cross aldol reaction

Q: Predict the major product. OH A) ساده воля B) H 1) CH3-S-CH₂ 0 0 CI-C-C-CI 2) Et N OH D) E) 1)…

A: In the given reaction sequence the first step is the oxidation of primary alcohol to aldehyde. When…

Q: 2. Reductive amination is a great "one pot" method for making substituted amines. Proposed a…

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Q: PQ-8. What is the major product of this reaction? Br CH3ONA CH;OH (A) (В) (C) (D) 20 PQ-30. What is…

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Q: Consider carbonyl compounds A– E attached  below. Rank A–E in order of increasing stability.

A: To check the stability of all the above carbonyl derivatives we have to check the inertness of the…

Q: ANS At

A: Carbonyl compounds react with azide in acidic conditions as shown in the following step.

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Q: 3 4 points NaCN CH3CN Br Predict the product of the reaction shown above. , SN2 CN , E2 CN , SN1 No…

A: Approach to solving the question: E2 (Bimolecular Elimination): This mechanism involves the…

Q: Propose a plausible synthesis of the compound on the left form the compounds on the right. &

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Q: omplete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or…

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Q: 1) For each pair of compounds below, predict the hybridization of the lone pair, and specify the…

A: Hybridization is the process of intermixing of atomic orbitals of similar energy to form hybrid…

Q: Present a plausible synthesis of the following transformation below. Explain

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Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 + МеОн HO, OMe cat.…

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A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Provide the reagents necessary for each step from the drop- down menus below. A [Select] B [Select]…

A: Step 1 : DEM reaction with NaOEt gererates anion. Step 2 : C-alkylation. Step 3 : Ester hydrolysis…

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.