(E) An aprotic solvent is best for Sn1 reactions as they tend to help stabilize carbocation intermediates.

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: Predict the main product of the reaction in Figure 10.

A: Alkyl bromide reacts with ammonia, a nucleophile to give a nucleophilic substitution reaction to…

Q: Considering these four types of alkyl halides, primary, secondary, tertiary, and methyl, which kind…

A: We know that SN2 reaction : the SN2 reaction proceed in one step and it is second order reaction it…

Q: How does the strength of the nucleophile affect an SN1 or SN2 mechanism?

A: Given reaction types,     SN1 reaction mechanism     SN2 reaction mechanism

Q: In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1,…

A: As per rule only three subparts can be answered.

Q: What would be the major product if they are reacted with the reagents in the second column?

A: Since, you have asked multiple subparts questions, we will solve the first three subparts questions…

Q: Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane

A: In this question, we will draw Complete mechanism for E2 Reaction.  You can see details Solution…

Q: alkylhalide in order of decreasing reactivity in an SN¡ reaction:

A: The order of reactivity of alkyl halides towards SN​1 reaction is-  Tertiary halide(3°) >…

Q: Assuming R = any alkyl group and LG = leaving group, for each carbon electrophile in the chart…

A:

Q: For the reaction shown, draw the transient product of one equivalent of reagent adding across the…

A: The given alkyne is converted into alkene (product A) in presence of 1 mol of H2,Pt

Q: Draw the curved mechanism arrows that show the SN2 reaction of phenoxide with chloroethane and draw…

A: SN2 is bimolecular substitution reaction , which occurs in a single step and in this case no…

Q: Which one of these is the most reactive in an E1 reaction? Explain.

A: E1 is the elimination unimoleculer reaction. LG is the leaving group and B is the attacking base…

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: We know that SN1, E1 and SN2, E2 mechanisms follow the first and second order kinetics respectively.

Q: Write the letters that correspond to the starting material ______ and the product ______ for the…

A: We have to determine the starting material and the product

Q: At which position in the final product is there an ethyl attached?

A: Given that : We have to identify the position of the ethyl group in the final product :

Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

A:

Q: Circle the major product in the E1 reaction of the following alkyl halides

A:

Q: Predict the product of the following substitution reaction?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: see the attached question and out of these 3 comounds, which one is the best dienophile ?

A:

Q: In an SN1 reaction, what are the Stereochemistry Consequences: (Retained, Inverted, Lost,…

A: The SN1 reaction is one type of nucleophilic substitution reaction.  Basically, There are two types…

Q: Choose the reagent(s) that would be most likely to complete this reaction. Br

A:

Q: Construct a three‑step synthesis of 1,2‑epoxycyclopentane from cyclopentanol by dragging the…

A:

Q: Draw arrows to show a typical SN1, SN2, E1 and E2 reaction

A:

Q: 4. Circle the molecule that would react fastest in an SN2 reaction. In addition, classify cach…

A: The molecules given are,

Q: For each pair, which compound would be more reactive in a S?1 type reaction?

A: Given : Reaction mechanism is SN1.

Q: Draw a detailed mechanism, showing appropriate bonds forming and breaking, for the reaction between…

A: The given reactants, cyclopentadiene and methyl acrylate undergo a Diels-Alder reaction, which…

Q: nydrogen and the leaving group have to be antiperiplanar in which reaction? E2

A: There are two types of elimination reactions.  First is E1 and other is E2.     (Dear student,…

Q: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Step-1 : 3-bromo-2-methylbutan-2-ol formation Step-2 : Epoxide formation Step-3 :…

Q: Draw curved fishhook arrows to show the movement of electrons in this step of the reaction…

A: In a free radical reaction mechanism, the homolytic bond cleavage takes place. During homolytic bond…

Q: For this mechanism, how come the iodine doesn't attach to a carbocation on the right (with the two…

A:

Q: а.) b.) с.)

A: Acetals on hydrolysis gives corresponding aldehyde or ketone and alcohols. Let's see here,

Q: 2. Draw the major product of this SN1 reaction. Ignore any inorganic byproducts. он HBr

A:

Q: How come in step 3, water doesn't attack the carbocation? Wouldn't it naturally want to immediately…

A:

Q: From each pair, select the stronger nucleophile. Q.)Cl2 or I2 in methanol

A: Given: Cl- and I- in methanol.

Q: For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure…

A: In unimolecular nucleophilic substitution reaction, the intermediate formed is carbocation. More…

Q: А. В. С.

A:

Q: . Complete the proper curved arrow mechanism for the reaction shown below. Br H-Br

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

Q: pts) Show any reaction that would involve the rearrangement of an intermediate carbocation.

A:

Q: From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

A: The species which make a covalent bond by donating a pair of electrons is termed as nucleophile.…

Q: final

A: Please find the file attached for explanation

Q: Choose the reagent(s) that would be most likely to complete this reaction.

A: Given: reaction of formation of 2-pentanol from pentene. To find: suitable reagent for this…

Q: explain why a polar aprotic solvent speeds the rate of an SN2 mechanism

A: A polar aprotic solvent is a solvent that lacks an acidic proton and is polar.  Polar aprotic…

Q: 2. Circle the member of each horizontal pair that undergoes the faster SN2 reaction with Na*N3 in…

A:

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: ?? Remember - can't use simple enolate/enol 7. for SN2 type reaction.

A: For addition to alpha to carbonyl compound, we have to convert that centre to nucleophilic centre.…

Q: Choose one example from the set of synthesis reactions in Model 1

A: In model-1 there is a different types of chemical reactions are given 1. Combination reactions ( set…

Q: NO2

A: The organic reaction takes place in many steps. These steps involve the use of various reagents.

Q: which term describes the next mechanistic step in the catalytic cycle of the heck's reaction

A: A multiple choice question based on alkene, which is to be accomplished.

Q: What is a correct mechanistic step of this reaction?

A: The given reaction is SN2  reaction because the  inversion of stereochemistry of reaction  occurs .…