Provide a synthesis  of  CH3CH2CH2 CH2 SH from any alkyl halide. Show the structure of all reactants and products.

Q: What reagent should be used to carry out the following reaction?

A: The reagent that can be used to carry out the above process is written as follows:

Q: phenol OH OH он NO2 dil. H2SO, NANO, NO2 OH OH он NO2 NH2 HN product C product D Paracetamol a.)…

A: Synthesis of paracetamol

Q: Draw the missing organic structures or select the missing reagents in the following multistep…

A:

Q: H,CH2C H,CH2C CH3 H,CH,C H,C H JAN JEN JIN JUN 22. produces an a-diketone upon reaction with cold,…

A:

Q: Do a retrosynthetic analysis on the following compound, ending withavailable starting material.

A: In a retrosynthetic analysis, in order to prepare the target compound, the precursor is identified…

Q: In the synthesis of 2-methyl-pentan-2-ol from pentan-2-one, the source of the nucleophile in…

A:

Q: Using the given starting reagents and benzene as the only source of carbon, perform the desired…

A: In the first step acetylene molecule will react with base NaNH2 and Cl2. acetylene chloride is…

Q: Which combination of reagent is appropriate for the following transformation? Ph OMe Ph HO.

A: Given transformation is,

Q: Please provide a way to synthesize the target compound using the reagents given below once Target…

A: The conversion reaction is given in the following step.

Q: Choose the most appropriate reagent(s) for conversion of ethyl acetate to acetamide. H OEt OCH2CH3 H…

A:

Q: Provide a detailed arrow-pushing mechanism for the following transformation: Me PHOH PhO. Et Мe Me…

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Q: H+ -H HO, (a) + 2 ELOH (b) HO.

A: ->alcohols have nucleophilic character hence , it can give nucleophilic addition reaction to…

Q: Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl…

A: The rate of nucleophilic substitution increases if the compound has high electrophilicity.

Q: 1.What is the best reagent to complete this synthesis? OA 1)???? CN 7.) NaCN.

A: Since you have posted a multiple questions in a single session, we are entitled to answer first…

Q: COOH COOH OH OH OH OH H3C H3C H3C" Br Select reagents from the table to perform this synthesis; only…

A:

Q: Propose an efficient synthesis process for this transformation. HO,

A: Williamson Ether Synthesis: Williamson ether synthesis is a type of coupling reaction for the…

Q: Which is a synthesis of 3-bromohexane? 1 eq. Br2 H2. Lindlar NaNH2 1 ед. HBr H2, Pd/C NaNH2 1 eq.…

A: Here in the given reaction, 1-butyne is converted to 3-bromohexane through a number of steps.…

Q: What reagent or reagents are needed to complete the following transformations? If more than one…

A: The conversion of the reactants to products are given below,

Q: 1. PBR3 2. Mg°, THF 3. dilute H30* НО OCH3

A:

Q: え 一X HO OH HO 人

A:

Q: Identify reagents that can be used for the following synthesis: ? C 1) HBr; 2) NAOH C 1) Br2, hv; 2)…

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Q: Devise a 4-step synthesis of the product from the starting material. CH3 1. reagent 1 2. reagent 2…

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Q: он 1. Pd'Ln, EtgN, MECN Me HO" 2. NABH4, MEOH 3. çI , ElgN, CH,Cl, Me

A: Step 1 : Heck coupling followed by isomerization. Keto to alcohol using NaBH4. O-acetylation of…

Q: Show how to convert each starting material into benzylamine in good yield

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Q: Aldehydes and ketones give additon reaction with a.phenylhydrazine b..hydrazine c.HCN d. All of the…

A: The detail solution is given below

Q: Give a reduction that you can use to synthesize benzaldehyde.

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Q: 14 Show the steps necessary to synthesize this compound by the Williamson ether synthesis. → phenyl…

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Q: Propose an efficient synthesis for the following transformation: (a)

A: Here we are required to find the reagent to carry out the following conversion

Q: Complete the multistep synthesis by indicating the needed reagents for each step. Please note: Ph -…

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Q: Propose a synthesis through a condensation, from compounds of 6 or less carbons

A: Given  synthesis through a condensation, from compounds of 6 or less carbons.

Q: .  identify the structure of A and B in the following synthetic scheme: Write out complete reactions…

A: By observing the nature of the reagents used,  we can expect ketone and imine as products…

Q: a. Which of the following reactions does not give the carbonyl product shown?b. Which of the…

A: Since, you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: What reagent or sequence of reagents is needed to complete the following transformation? .CO2H CO2H

A: KMnO4 is a strong oxidizing agent. It can be used to oxidize the side chains of the aromatic rings…

Q: KOH/H2SO4

A: Given reactions, (1)       (2) ethyl propyl ether synthesis

Q: Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene…

A: When a aldehyde or ketone is reacted with 1,2- diol , acetal or ketal is formed. When 2- butanone is…

Q: Choose the best reagent to complete this reaction. Assume an acidic work up. NH2 NH2

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Q: Choose the appropriate reagent to carry out the following transformation TsN TsN 1. 1) 9-BBN; 2)…

A: The given reaction is as follows and follows the Suzuki coupling mechanism.   STEP1 -…

Q: HO-

A:

Q: What is an appropriate stepwise synthesis for 1-pentanol from butanal? NABH4/CH;OH; PB13; Mg/ether;…

A: 1) Last reaction reagent sequence is not correct because no solvent used with NaBH4 and no acidic…

Q: Complete the following malonic (di)ester synthesis by showing all reagents and reaction conditions…

A: The given reaction is,

Q: 8) Provide the necessary reagents to complete the following syntheses. OH H3C" CH3 CH3 CH3 Br NH, HO

A:

Q: Draw the missing organic structures or select the missing reagents in the following multistep…

A: Here, we have to draw the missing organic products and the missing reagent for the given multistep…

Q: How to synthesis compound 1 from compound 2? OMe t-Bu MeO2C MeO¿C но 1

A: For the synthesis of compound 1, the starting material, which is compound 2, is reduced selectively.…

Q: What reagent would you use to do this reaction? H2N HO. O a) HgSO4, H3o* b) KMNO4 O c) Cro3 d)…

A: KMnO4 strong oxidizing agent it cam oxidize almost all compounda even alkyl groupa to carbozylic…

Q: Ph OMe Ph HO

A: Given transformation is,

Q: Which reagents would you use to perform reaction B?a) PBr3.b) p-toluenesulfonyl chloride.c) SOCl2.d)…

A: The given reaction is shown below:

Q: 4. Give a short, efficient synthesis of the target compound from the indicated starting material and…

A: The required synthesis is as follows:

Q: 1. Diagram a scheme for synthesizing the compound on the left from the compound on the right. Show…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Identify the reagents needed to complete this multistep synthesis.

A: Given that : We have to identify the reagents needed to complete the following multistep synthesis :

Q: How to Converting an OH Group into a Better Leaving Group?

A: Alcohols are the organic compounds which contains an -OH group. This group is not a good leaving…

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.