Which of the following reactions in each pair will occur faster?

Q: Compare the following pairs of molecules and determine which one is the stronger nucleophile

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Q: Which of the following is the rule which states that the more substituted product is the major…

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Q: Which of the following species cannot be considered a nucleophile?

A: A. Carbocation is electron deficient. Therefore it act as electrophile. B Oxygen is having lone…

Q: Explain why the following reaction sequence will not occur:

A: -NH2 is an electron donating group. Hence, it increases electron density more on ortho and para…

Q: What is the rate-determining step in the following reaction?

A: Given: To find: the slowest step in the reaction mechanism.

Q: Going down a group, consider the halides: Of the halides shown, which is most basic? Of the halides…

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Q: Rank the following substrates in order from slowest E1 reaction rate to fastest:

A: We have to arrange order for slowest E1 reaction to fastest E1 reaction.

Q: By following the curved red arrows, draw the product(s) of each of the following reaction steps.…

A: a. In accordance with the movement of electrons in the above reaction, bromine atom was detached…

Q: d. Consider the following secondary halides. Changing the leaving group from fluoride to bromide…

A: Halides are good leaving groups. The tendency of the leaving group increases as the size of the…

Q: at product will result from the reaction shown? (Just mention the class of compound not the…

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Q: Which one should be considered the major kinetic product of the following reaction?

A: Alkadienes electrophilic addition reactions 1. 1,2-addition : At lower temperature conditions…

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction can be drawn as

Q: Which is the better nucleophile, A or B?

A: This question is related to the topic electrophilicity and nucleophilicity. A nucleophile is species…

Q: Which is faster, why? # of products for each reaction? What is the mechanism of each reaction?

A: Given reaction is William son synthesis reaction in which nucleophile attacks on the alkyl…

Q: Which of the following is most likely an intermediate in the following reaction?

A: As concentrated sulfuric acid is a strong oxidizing agent, it oxidizes some of the alcohol to carbon…

Q: Do the reactions below proceed in good yield from left to right as shown?

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Q: 9.42 Did the overall reaction shown here occur by an SN2, Sn1, E2, or E1 mechanism? How do you know?…

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Q: Draw the MAJOR product(s) of this reactions:

A: We have given the organic reaction we have to find the major product of the reaction.

Q: Predict the main mechanism that occur for the following reaction

A: Nucleophilic substitution reactions the electron-rich nucleophile attacks on a positively charged…

Q: Which nucleophiles will add to the following conjugated enone at the A carbon?  Which will add at…

A: The compound given is,

Q: what are the products of this reaction based on the arrows?

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Q: Draw the major product of the each of the reactions in the presence of acid and water and the…

A: Potassium dichromate is the stroger oxidising agent which oxidises primary alcohol into direct…

Q: Which will react slower in polar protic solvents

A: Polar protic solvent is polar solvent.

Q: What is the final product (D) of the following reaction sequence?

A: In the first step, p-chloronitrobenzene reacts with Fe/HCl followed by NaOH to form p-chloroaniline

Q: Draw all products of these reactions AND explain which is the major product.

A: Elimination reaction :   When two substituents release from an organic group leading to an…

Q: Give clear handwritten answer- identify fastest heterolysis step !

A: To identify fastest heterolysis step

Q: Which nucleophile gives the highest overall reaction rate

A: Substitution reactions in which one nucleophile is replaced with another nucleophilei called "…

Q: Draw the step-by-step mechanism using curved arrows of the following reaction in acidic condition.

A: NaOCl in an acidic medium acts as an oxidizing agent. The given reactant is;

Q: The reaction shown here is called the pinacol rearrangement. A carbocation rearrangement is believed…

A: When vicinal diols are treated with acids, they can be rearranged to give aldehydes or ketones. This…

Q: Which of the listed conditions and nucleophile/s will open the epoxide at carbon A? Which will open…

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Q: Which sn² reaction is each pair is faster

A: Given Two SN2 reactions varied by two different nucleophiles OH- and CH3COO-

Q: How do we ban this compound with its reaction mechanism

A: The above given compound is Aspartame. It is used as artificial sweetners.

Q: Which face (axial or equatorial) undergoes reaction with sodium borohydride faster?

A: Sodium borohydride is reducing agent. Sodium brorohydride reacts with ketone to form alcohol.

Q: H

A: These all are derivatives of carboxylic acids. The rate of hydrolysis depends on two factors –…

Q: Which of the following will undergo hydrolysis the fastest?

A: Nucleophilic substitution (SN)  type reactions in acid derivatives : Acid derivatives :  1. Acid…

Q: please explain what happens in this reaction mechanism. be as DETAILED as possible. acetylene +…

A: Br2 is a covalent compound, there is no charge separation. But during the reaction there is a…

Q: Please help me draw the MAJOR product(s) of the this reaction.

A: It is an example of Friedal craft alkylation reaction

Q: Which out of the given nucleophiles will open the following epoxide at the A carbon? Which will…

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Q: Circle the most acidic position in each molecule that could be deprotonated to give an enolate.

A: Enolate is an organic anion generated by the deprotonation of carbonyl compounds. Enols are a…

Q: Which of the folowing is the product for the given reaction?

A: Benzene undergo electrophilic substitution reactions  In general g oups substituted on benzene are…

Q: Choose the two major products of the following reaction.

A: The given reactant i.e. 2-bromopentane is a secondary alkyl halide and the reaction is carried out…

Q: Draw the complete, detailed mechanism for the reaction shown here and give the major product. CH3I…

A: The reaction of 4-methoxyhex-1-en-3-amine with CH3I followed SN2 mechanism results in the formation…

Q: Which reagent(s) will result in the nucleophile attacking the more substituted side of an epoxide?…

A: The question is based on the concept of organic reactions. It involves ring opening  of the epoxide…

Q: Which of the following is an (are) intermediate(s) in the mechanism of the reaction shown below.

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Q: Draw the products of attached reaction, and state whether the reaction is faster or slower than a…

A: The carbonyl group withdraws electron density from the ring deactivating it towards electrophilic…

Q: Draw the complete, detailed mechanism for the following reaction along with the major product. Cl2…

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Q: Which will react faster??

A: Sn2 reaction is  bimolecular nucleophilic substitution reaction

Q: The geometry favors the E2 mechanism because it will promote the effective

A: The leaving group is always anti-periplanar to the hydrogen that is removed on the β carbon. in…

Q: Rank the nucleophile strength of the structures from weakest to strongest.

A: In this question, we have to give Rank the nucleophile strength of the structures from weakest to…