including all resonance isomers for intermediates (show electron flow) for the Friedel-Crafts reaction done in the lab.  NOTE:  It is likely the mechanism from reactants to only 1-t-butyl-2,5-dimethoxybenzene

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A: Epoxide undergo ring opening in presence of acid and a nucleophile through SN1 pathway.

Q: HNO, H,SO, KMno, H (b) 1. Fe, HCI 2. NaOH NaNO, HCI (4) HO, heat (e) (a) CHOH, H mehybaraben

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A:

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Q: 3) + H. NaOH Give the mechanism and product. ?

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Q: True/False)  The use of sodium iodide in acetone promotes SN2 mechanism for alkyl halide resulting…

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Q: 2) When molecule 2 is treated with HBr and peroxide one major product is formed. Based off of the…

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A:

Q: What change, if any, would you expect if the aromatic substituents were in the ortho position to,…

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Q: Give the major product (16) and the mechanism for the elimination reaction given below.

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A: The answer is given as follows

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A: The given reaction is an example of Horner–Wadsworth–Emmons (HWE) reaction.In the given reaction the…

Q: 4. A student performed the following sequence of reactions: an oxetane opening, followed by a…

A: As per the given data, 1 H- 1.25 3H t 1.28 6H s 1.65 2H t 2.60 2H t 3.45 2H t 7.2- 7.3…

Q: Give the major product(s) and mechanism for the following reaction (if more than one major product,…

A: The product formed when Phenol reacts with concentrated H2SO4 is majorly depends on the temperature…

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Q: OC is the most likely product of the following E2 reaction? CH₁ Br Br NaOCH₂CH₂ CH,CH₂OH CH₂ CH₂

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Q: 4. For each of the following reactions: name the mechanism (one of Sn2, SN1, E2, Et) then draw a…

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Q: 1. Check the following reactions' starting materials, reactives and solvents. Considering these…

A: The detail solution of reaction is provided below in attach image.

Q: d. Draw the elimination product that would form upon reaction of (4S)-1-bromo-4- methylhexane with…

A: The reactant used is (4S)-1-bromo-4-methylhexane. The reagents used are (CH3)3COH and (CH3)3COK.

Q: In the electrophilic aromatic substitution – sulfonation reaction, Indigo carmine absorbs which…

A: The absorbance spectrum shows the interaction of different dyes with light. The peak in the…

Q: 2. Draw the structure of the missing product or reactants: CH,=CH, ? + а. H2C=HC-CH=CH, C=N ? b. с.…

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Q: out the mechanism (intermediate/transition state) for this CH₂ Br LIOH E₂ 11. For the following use…

A: For the E2 reaction to the leaving group and beta-H should anti to each other

Q: 10. Write out the mechanism (intermediate/transition state) for this reaction. Indicate…

A:

Q: 4. Show the detailed mechanism for the following reactions. Label steps (Sn2, protonation..), and…

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Q: c) After treatment of 2-methylpropene with peroxyacetic acid (CH3CO3H), write the mechanism with…

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Q: Question 1. Provide a full, rigorous mechanism for the transformation below. Include all possible…

A: Given reaction is Sulfonation reaction. Sulfonation reaction is a type of Electrophilic Aromatic…

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Q: 2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and…

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Q: help please answer in text form with proper workings and explanation for each and every part and…

A: reaction is a Friedel-Crafts alkylation where cyclohexene reacts with H₂SO₄ to form a cyclohexyl…

Q: stituted a In the problem-solving feature below, methylcyclohexanone was seen to react at its…

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Q: OH Н Ill CH3 :O: CH3

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Q: 7. Draw the mechanism and predict all major regiochemical and stereochemical products of the…

A: The objective of this question is to draw major regiochemical and stereochemical products of the…

Q: When an NMR spectrum is taken of the molecule below, there is the expected 5H in the aromatic…

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Q: Provide the full mechanism for the Friedel-Crafts Acylation reaction in the first step of the scheme…

A: The Friedel–Crafts acylation reaction is named after Charles Friedel and James Mason Crafts who…

Q: a multi-step synthesis for the indicated 1,3,5-trisubstituted benzene only using reactions discussed…

A:

Q: Propose a plausible mechanism using curved arrows that shows the 10. formation of product A only.…

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Q: 4. The issue with enol/enolate syntheses is that a lot of the starting materials and products have…

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Q: The

A: Ketone react with ethanol then we get acetal product. First ketone protonated by the gain of H+ then…

Q: Shown below are two reactions; Reaction 1 is a Friedel-Crafts acylation while Reaction 2 is a…

A: Friedal crafts acylation and alkylation both are electrophilic aromatic substitution reaction.

Q: Draw two complete elimination reactions including mechanisms (Zaitsev and Hoffman products) of 2 -…

A: Zaitsev rule: During elimination reaction, the elimination product is the one which has more…