Explain and provide the mechanism of the reaction. Name the final product with the assignment of configuration.

Q: Provide a plausible, stepwise mechanism to account for the following transformation. Use curved…

A: The mechanism can be shown as:

Q: Complete the following sequence of reactions by indicating the missing reagent(s). Also, show the…

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Q: Write the complete stepwise mechanism of the following reaction. Show all electron flow with arrows…

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Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition- elimination…

A: The curved-arrow mechanism to account for the given nucleophilic addition elimination reaction can…

Q: give the major products of each reaction

A: We have given three organic reactions.  Major product : the major product of reaction is the product…

Q: Complete the following reaction scheme. Give all product(s) and indicate major or minor and any…

A: Facts: Organic compound having OH, alkene .. + acid , then first form stable Carbaocation. After…

Q: Predict the structure of the product formed (with correct stereochemistry) for each of the following…

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Q: Give the reaction conditions which could be used to bring about the transformation shown in two…

A: Oxidation and reduction are the key steps here. These steps will result in our desired product.

Q: write the major carbon containing product of the reaction. and whether it id racemic or optically…

A: As there are more than three parts to this question. We are solving the first three parts for you,…

Q: What are the groups towards meta position give examples and what its mechanism ?

A: The meta-directing group generally are the electron withdrawing group that direct the upcoming group…

Q: (a) Indicate the following alkenes in order of increasing stability. Justify your answers.

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Q: The substitution reaction below forms two ethers (which are consitutional isomers). Which ether is…

A: Various reactions are studied in organic chemistry. Every reaction is guided by some specific…

Q: Provide a note on Peterson syntheses, with suitable example and mechanism.

A: Peterson synthesis is synthesis of olefinic double bond from carbonyl using α-silyl alkane.

Q: (1R,2R)-1-Bromo-2-methylcyclopentane is subjected to reaction with methanol. Give the product(s) and…

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Q: 3. Complete the following reaction scheme. Give all product(s) and indicate major or minor and any…

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Q: Provide the structure of the product(s) with stereochemisty if appropriate. If multiple products…

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Q: Give a mechanism that accounts for the organic products of this reaction. Your mechanism must…

A: In SN2 reaction there is inversion in configuration. This is because nucleophile attacks from the…

Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: Which double bond is more reactive in the molecule below? Explain. Draw the major product expected…

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Q: Br H;C. .CH3 `CH3 H

A: A<C<D<B This the order of decreasing reactivity for E2 elimination

Q: The transformation takes place via two sequential pericyclic reactions. Identify the two reactions…

A: Given & To find:-

Q: Illustrate the mechanism of forming alkynes from a 1,2-dihalide and a vinyli halide. Show…

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Q: Provide the reaction (reactants -> products) with detailed mechanism for the following, with AlCl3…

A: Since you have asked a question with multiple subparts we will answer the first three for you. To…

Q: Give the structures of compounds A through D in the following series of reactions. Show…

A: Structures of A and B are shown as follows: The configuration of A and B is same as of the starting…

Q: please explain clearly and in detail. thank you! 2-butene reacts with NBS yields and forms two…

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Q: Br Ph3Sn O3 K AIBN then NaBH4 Identify compounds J and K. Draw a curved arrow mechanism that…

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Q: i. aliphatic starting material ii. Он NO2 ČN

A: Given is retrosynthetic analysis problem. In solution blue arrow are for retrosynthethesis and pink…

Q: Below is a schematic representation of possible reactions that Compound X can undergo. Use the…

A: Hi, since there are multiple subparts posted. we will provide you with answers for the first three…

Q: Which of the following alkenes will give the * same major product upon reaction with HCI? A A & B B…

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Q: Predict the MAJOR product(s) of each reaction or sequence of reactions. Show stereochemistry where…

A: Nucleophilic substitution reactions (NSR) :  These are two types 1. SN1 : Unimolecular…

Q: Rank the following carbocations in terms of stability from lowest to highest. to A B C D

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Q: Heterocyclic compounds plays an important role in our daily life. They are mainly used in…

A: The structure of thiophene: A halogen group can reacts with thiophene to form a suitable compound.…

Q: addition of hbr to a double bond with an ether (-or) substituent occurs regiospecifically to give a…

A: Addition of HBr to the double bond gives electrophilic addition reaction. During this reaction, a…

Q: Br NaOCH3 CH3OH

A: In presence of sodium methoxide , where methoxide anion acts as nucleophile and carry out…

Q: Below is a schematic representation of possible reactions that Compound X can undergo. Use the…

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Q: On reaction with HC1, one of the trimethylcyclohexanols shown below furnishes a single product; the…

A: In the mechanism, first, the protonation of -OH takes place, then the removal of H2O forms a…

Q: (1R,2R)-1-Bromo-2-methylcyclopentane is reacted with sodium methoxide. Given the product(s) and show…

A: An elimination reaction in organic chemistry is a reaction where a base abstract An acidic proton…

Q: Predict the major organic product for the following reaction. You do not need to account for…

A: The solution is given below -

Q: 1) NaH 2) 3) H*, heat

A: NaH (sodium hydride) is a strong base. It abstracts a proton from more acidic hydrogen. The…

Q: Reaction of the cyclic product with a nitron (see below) yields a mixture of heterocyclic…

A: Given reaction:

Q: Give the major produc

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Q: give the major produc

A: 1. Baeyer -Villiger oxidation :  Ketone and per acid with acid reagent rearranges to esters is…

Q: Predict the major product of the following reactions. If it is possible, write all stereoisomers.

A: When terminal alkyne upon treated with strong base like sodamide (NaNH2) gives a carbanion by loss…

Q: Provide a reasonable stepwise mechanism for the following transformation. Show the structure of any…

A: Solution: We know all kinds are are electron reached due to buy bonds so they can act as nucleophile…

Q: Classify the following sigmatropic rearrangement and determine whether it takes place readily under…

A: In Sigmatropic rearrangement a sigma bond undergoes rearrangement which is flanked by π-electrons.

Q: Giving your reasoning, rank the following dienes in order of increasing reactivity reaction. i) ii)…

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Q: + COOH HOOD. A

A: Here we have to write product formed , it's stereochemistry and it's name in the following Diel's…

Q: Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr. Give a…

A: Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr. A…

Q: N 애 웅도

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Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.