H;O H,SO, (cat)

Q: Show the mechanism (arrow pushing) for the following reaction: 1. NANH2 2. Br

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. Hint: NaOBr is in solution along…

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Q: 2. Provide a detailed mechanism for the following reaction: Br NBS light

A: Allylic bromination of alkenes can be achieved by using N-Bromosuccinimide (NBS) in the presence of…

Q: H2N- -ОН HO SOCI, Ме ОН Ме Ме

A: Given,

Q: BOH)2 Pd(PPH3)4 Br K2CO3

A:

Q: Propose a plausible mechanism for the following reaction: (H,SOJ

A: Interpretation -  To tell about the possible reaction mechanism for the following given reaction…

Q: Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution,…

A: This reaction is diazotization followed by substitution some rearrangement and elimination reaction…

Q: H2SO4 но H20

A: Hydrolysis of ester into acid and alcohol.

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. TSOH, A + H20

A: acidic Aldol mechanism  with full arrow steps involved in step-2

Q: 4. Draw mechanisms for the following reaction (or sequence of reactions): HO.

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. H-A + МеОН МеО HO

A: In the conversion of organic reaction the movement of electron density from one atom to another atom…

Q: When allyl bromide is refluxed with magnesium metal in ether solvent, the product formed is…

A: At first grignard reagent is formed, and it become nucleophilic, so further attack in allyl bromide…

Q: Propese the below epoxide Starting with cycloheptanone a mechanism for HC CH3 SCH3 CH3 CHs

A: Detail mechanistic pathway is given below

Q: Draw the major product and state wheter the reaction is SN2, E2, SN1, or E1

A: 1. Sodium tertiary butoxide is bulkier alkoxide ion , it acts as like base hence it abtsract beta…

Q: Suggest likely a mechanism for the following reaction: PPO OPP- CH3

A:

Q: 1. LDA (slight excess) 2. CH3CH2I

A: LDA is a sterically hindered strong base. LDA is the best reagent to synthesize the kinetic enolate.…

Q: OH H2SO4 (cat.) H20

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Q: NO2 HNO3 H2SO4

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Q: What is the predominant mechanism of the reaction below?

A: Elimination reaction :   Inpresence of strong base , heating conditions elimination reactions…

Q: Suggest a mechanism for the following reaction. Explain why NaB(CN)H3 is preferable to NABH4 as…

A: We have to suggest mechanism for the following reaction in step 2

Q: D. Provide reasonable mechanisms for the following reaction H NaOH, H₂O, A

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: Show each step using curved arrow formalism.

A: The given reaction is :

Q: (a) Draw the structure of molecule (A) that is in equilibrium with molecule (B). (b) Show a…

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Q: Draw a plausible mechanism for the following transformation. H2SO4 + NH,NH2 + 2H20

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Which of the following is most prone to hydration (acid-catalyzed reaction with water)? a. b. C. d.…

A: Aldehyde which is most prone to hydration is.

Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount).

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Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. H-A LOH MeOH Meo

A:

Q: Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution,…

A: Applying concept of elimination, and rearrangement reaction based on appropriate stereochemistry of…

Q: Но OH + H+

A: Answer is explained below. The given reaction is :

Q: H2NNH2, KOH Hао, heat

A:

Q: Write the complete stepwise mechanism for the reaction below: (Non-anonymous question Ⓒ) OH HC1 OCH3…

A:

Q: A B C heat Na NH3 1) 03 2) DMSO reductive workup OH O H

A: Since, you have multiple subparts questions. So, I will solved first three subparts questions for…

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. H-A H2N HO HAN

A:

Q: provide a reasonable mechanism for the following reaction CX НО, OH H₂SO4 (cat)

A: Basically this reaction ia used in protection of aldehyde and ketone in order to prevent the…

Q: a) ОН ОН b) CI HO

A: Here we have to prepare the following compounds from the given starting material in multistep…

Q: Suggest a reasonable mechanism for the following reaction Ph OCH3 Ph. OCH3 FeCla Ph Ph OCH3

A: FeCl3 acts as a catalyst. It helps in removal of methoxy group to produce electrophile. Attack of…

Q: Provide a mechanism for the reaction below: H H. HCI

A: Chloromethylation is reaction of aromatic rings with formaldehyde and hydrogen chloride. The…

Q: 5. Provide an adequate route (reaction scheme) for the following reaction

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Q: H OH + H-CI = `CH, CH,

A:

Q: "ropose a mechanism for the following reaction. но H,SO, + H,0

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Q: hv . 3D

A:

Q: Propose a mechanism for the reaction in Question 2.1.3.

A: In this reaction (4+2) cyclo addtion takesplace Diene and dienophiles reacted to give a cyclic…

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

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Q: Draw a detailed mechanism for the chlorination of benzene using Cl2 and FeCl3.

A: The general reaction is as follows,

Q: Write a detailed mechanism for the following reaction. он Он H,SO4, H2O ÓH но

A: All steps mention in hand written solution.

Q: HO OH H+ to

A:

Q: 5) Provide a reasonable arrow-pushing mechanism for the following reaction. H20 H2SO4

A:

Q: 4. Provide a detailed, stepwise mechanism for the transformation shown below. 1. NaOEt CO2 Et 2.…

A: the given reaction is: The step wise mechanism for this is given below:

Q: 17. Provide a curved arrow mechanism for the following transformation. Br NaN, DMSO

A: As shown in the reaction, the rection follows SN2 pathway because the product is inversion in…

Q: What is/are the best reagents (i.e., chemicals for the box below) to carry out the following…

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