4.) Write the letters associated with the compounds that will not undergo a rearrangement in a Friedel-Crafts reaction. Write your answers here: B) A) CH;CI E) .CI D) II

Q: The major product of the following reaction is он H,SO, heat

A: First lone pair of OH will attack on H of H2SO4. See the written solution.

Q: Here in Chapter 23, we learned that aniline becomes highly deactivated in the presence of a strong…

A: Given: Aniline is highly deactivated in the presence of a strong Lewis acid, due to coordination of…

Q: HEAT

A: In this question, we want to draw mechanism for this reaction.  You can see details mechanism below.…

Q: write one name reaction with mechanism . Give four example of this name reaction with mechanism of…

A: So here as you asked for any one name reaction , so I will discuss Mannich reaction here which is…

Q: duce this regiochemistry in elimination reaction. Br

A: As we know,  In E2 mechanism polar aprotic solvent is required and strong base and heat is also…

Q: a) Describe the general steps in the mechanism for an SN1 reaction and an SN2 reaction. b) Discuss…

A: The reaction in which an atom or group is substitutes by any other atom or group is known as…

Q: Please provide a detailed mechanism (with arrows) for this reaction.

A: Here we have to provide the mechanism of synthesis of sulfathiazole-

Q: Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inammatory, and…

A: a). Resonance structures for the radical that results from homolysis of the OH bond: The radical…

Q: (A) Provide the major organic product for the reaction below (B) Would the product be optically…

A: Sugar undergoes oxidation reaction in presence of HNO3 . Both aldehyde and alcohol group is oxidis

Q: [H] N-H

A:

Q: Would the SN2 step between HO- and CH3Cl be allowed if HO- were to approach CH3Cl from the same end…

A: Given reaction,              SN2 step between HO- and CH3Cl

Q: Provide an arrow pushing mechanism for the following reaction. Make sure to include initiation,…

A: It is a radical addition reaction. It is first explained by Karasch. It is also known as Karasch…

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: draw the mechanism and label makor resonance structure catalytic H,50, HO molecule A molecule B

A: This question is asking the basic concept of resonance effect. We know that,  Resonance always…

Q: List the Unimolecular substitution (SN1) mechanistic steps (as discussed in the problem solving…

A: The correct explanation with example SN1 reaction is given below

Q: c. Please rank the following radicals in order from least to most SELECTIVE: A В C D Please explain…

A:

Q: Give a detailed explanation on the reaction of tje compound and its mechanism and why did it happen.…

A: Explanation for the reaction of butanol with HBr.

Q: One the molecule below, which hydrogen atom would be abstracted at the fastest rate by a bromine…

A: The molecule given is,

Q: What would be an appropriate term to describe molecules B and C? in A В Me `Me Me resonance…

A: Molecule A is conjugated. B and C are skip diene

Q: Write a detailed mechanism f

A: Protonation of alkene  Attack of alkene as nucleophile (intermolecular reaction)   Deprotonation

Q: Analyze the reaction below, and determine the reagents necessary to carry out the conversion. Be…

A:

Q: Please explain the following clearly. 1.Benzene undergoes electrophilic aromatic Substitution rxns.…

A: As per our guidelines, we can only solve one question at a time please post other questions as next…

Q: NH2 Br 1

A: In the given chemical reaction the amino group attached with the benzene ring is replaced by the…

Q: Please write the mechanism for the following reaction.

A:

Q: 3. Consider the following Diels-Alder reaction: a) Draw a detailed mechanism for the reaction and…

A:

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: (a) Why cyclohexene and cyclohexa-1,3-diene are expected to undergo addition reaction but benzene…

A: Organic compound undergoes electrophilic substitution reaction in presence of electrophile. Electron…

Q: from b.

A: For this transformation, oxidation of the alkene is carried out.

Q: 1) Which one more reactive to word nucleophilic substitution P- nitro toluene or O- ethyl toluene ?…

A: P-nitro toulene will be more reactive towards nucleophilic substitution than O-ethyl toulene because…

Q: And Allyl / Phenyl compound are most reactive towards SN2 because of resonance stabilization. then…

A: SN^2 reaction is a single step process. SN^1 reaction is a two step process. SN^1 reaction involves…

Q: What is mechanism of ether cleavage  Is this cleavage following SN1 or SN2 ? Give your explanation

A: Ethers show nucleophilic substitution reaction.

Q: from and alcohol of two carbon or less Cl

A:

Q: What is the best way to remeber the differences between Sn1, Sn2, E1 and E2 reations?

A: The best way to remember differences between SN1,  SN2, E1 and E2 reaction is that

Q: write one name reaction with mechanism . Give four example of this name reaction with mechanism of…

A: It is a rearrangement reaction. This reaction is [3,3] sigmatropic reaction. It is rearrangement of…

Q: Write o o mechanism to hronsform Compound A to B NH2

A: For reaction 1, we will use aniline (which is used as polymer)  For reaction 2 and 3, we will use…

Q: Complete this concept map to summarize all epoxide reactions: CH3 CH₂ НО. Weak Nuc, H₂O+ CH3 H3C 1.…

A:

Q: Fill in the blanks: The rate of the SN1 reaction depends on the and therefore involves kinetics.

A:

Q: 3) If the product of an SN1 or Free radical reaction contains a stereocenter then a _______________…

A: Nucleophilic substitution reaction are of two types viz. SN1 and SN2. Nucleophiles are nucleus…

Q: her question will stve this respo on 18 Which aly chioride reacts fastest in S2 reactions?

A: The SN2 reacction is most favored in those alkyl halides which forms less stable carbocation.…

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: The reaction of aniline with benzoyl chloride (an acid chloride) produces a mixture of two products,…

A:

Q: Draw a detailed arrow pushing mechanism for the following reaction. In the rate-determining step…

A:

Q: b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bond cleavage…

A:

Q: B D Write the letters that correspond to the starting material and the product for the mechanistic…

A: In this question, you give the letters for starting material and Product ( on the right side energy…

Q: ? CH, Hint Remember that overalkylation is a problem when it comes to Friedel-Crafts

A: Friedel-Crafts alkylation is the process of replacement of an aromatic proton by an alkyl group and…

Q: (Chapters 5–13) For each of the following, 14. a. Label the reactive features, highlight the most…

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

Q: What happens to the stereochemistry during and SN2 reaction? Why? Provide a reaction to illustrate…

A: