Propose a plausible mechanism using curved arrows that shows the 10. formation of product A only. Make sure to include all resonance contributors of the sigma complex and circle the most stable one. Lastpredict the second product of this reaction. OH OMe OMe H,SO, (A) (B)

Q: Write the complete mechanism with arrows of the following reaction. A

A: This reaction is a [1,3] cycloadditon reaction.The mechanism is as given below.

Q: Why we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the…

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Q: 3. Consider the electrophilic aromatic substitution reaction below. Draw three resonance structures…

A: More stabilized and Compound  with every atom has complete octet shows most contribution towards…

Q: NaOEt ELOH elimination product 8. Br

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Q: Ph. OTs OTs NaOH NANH, ? ? NaOH ? A В C Ph. CI NaOH dilute NaOH ? D

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Q: 1. For the transformation below, provide a detailed arrow-pushing mechanism. If intermediates occur…

A: The given substrate to you, has a acidic hydrogen and a good leaving group -OEt. Thus to find the…

Q: v.. Using curved arrow notation, propose a detailed mechanism that is plausible for the following…

A: This is an example of formation of bromonium ion followed by intramolecular SN2 reaction.

Q: 1) Write a detailed, stepwise mechanism for the following reaction. In your mechanism, provide three…

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Q: 2. а) Predict possible product for each transformation. i. EtO,C. NaOEt ii. OCH3 OCH3 ii. СНО MENH2,…

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Q: Consider the following reaction below. Which of the following choices has the con sequences of…

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Q: Both compounds A and B below give the same carbocation intermediate C in the SN1 reaction. However,…

A: In this question, we will Identify which Compound ( A or B ) give carbocation intermediate ( C )…

Q: draw the major organic product generated in the reaction below. Pay attention to Regio and…

A: A process that favors bond formation at a particular atom called regioselectivity. solution i)…

Q: Draw a plausible arrow pushing mechanism for the reaction below. You must use the exact structures…

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Q: Draw the major organic product generated in the reaction below. Pay particular attention to regio-…

A: The answer is given as follows

Q: Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is…

A: Alkyl diazonium salts are the excellent leaving group because R- N2+ because nitrogen is an…

Q: Provide a complete mechanism for the following reaction. Pay close attention to details, including…

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Q: Add curved arrows to draw the second part of the mechanism: tautomerization of an enol to a ketone.…

A: Given the first step of this reaction is the electrophilic addition of deuterium (D).  Second step…

Q: 3) Give a complete, detailed mechanism for the following transformation. C, HCI HCI

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Q: propose a synthetic route to this structure that includes at least one C-C bond formation step.

A: 2 -Methylbutanoyl chloride can be synthesized as given below.

Q: Next, provide a reasonable mechanism for product formation using appropriate curved arrow notation.…

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Q: Complete the Reaction below by providing both major and minor products, circle the major product.…

A: Given reaction is :  Complete the reaction and provides the major and minor products ?  The given…

Q: 2) Propose a set of reaction conditions to most efficiently carry out the following transformations.…

A: Detail mechanistic pathway is given below to carry out the following conversion with appropriate…

Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount).

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Q: Problem attached

A: The organic reactions are carried out with the help of specific reagents. Every reaction is guided…

Q: Predict the major product in the following reaction. Be sure to draw it with well-defined…

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Q: Propose a mecahism for the following reaction and include all relevent reagents (you may use any).…

A: This is a multi step synthesis reaction . By using the starting material with various reagents we…

Q: Br NH2 NANH2 NaBr

A: The reaction of bromobenzene with sodium amide results in the generation of aniline and sodium…

Q: With reference to the following reaction scheme: LIAIH4 Et,NH HCI (cat.) A C3H180 B C12H25N Me Но…

A: We have to draw the structures of the compounds A-D.

Q: 5) Provide a complete and detailed mechanism for these transformations. OH heat, acid +

A: We have to predict the mechanism for given reaction.

Q: 4. For the following reaction, draw a reasonable mechanism showing stereochemistry Br-Br

A: Reaction of of cyclohexene with bromine:

Q: H2O, H2SO4 H9SO4 A. В. С. E. None of these choices is correct. D.

A: In presence of HgSO4 and H2SO4 , H2O ,oxymercuration-demercuration reaction is carried out and…

Q: When drawing organic chemistry mechanisms with NaOCH3, do we automatically dissociate it into Na+…

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Q: Carbocation rearrangement of the cation on the right gives: A) B) D) two of the above

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Q: (i) Write both reactions using bond-line presentation and, using arrows providing a mechanistic…

A: Sn2 reaction is bimolecular substitution reaction.

Q: CI OH

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Q: 1) a) Propose a detailed mec major product. Please include: 1) a perspective diagram of the…

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Q: Draw the major organic product generated in the reaction below. Pay particular attention to regio-…

A: Given that : We have to draw the major product for the following reaction :

Q: If Zaitsev's rule does not apply and the base is bulky then how will the product look?

A: Bulky base like  potassium acetate will abstract beta proton from less hindered carbon to form less…

Q: 9. Draw a complete, detailed mechanism for the reaction below, and product(s). CH,OH NaOCH3

A: Ester are derived from substitution reaction of carboxylic acid and an alcohol, they are volatile…

Q: Aromatic heterocycles can undergo electrophilic aromatic substitution like benzene. Groups attached…

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Q: 3. Consider the electrophilic aromatic substitution reaction below. Draw three resonance structures…

A: Here we have to explain the cause major product formed in the bromination of anisole in the…

Q: OH H2SO4 H20

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

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Q: Draw the major organic product generated in the reaction below. Pay particular attention to 1)…

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Q: Br HOCH,CH3 :Br: OCH,CH3 Draw the product(s) of the following reaction by following the curved…

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Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

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Q: CH3 .CH3 Br H. H.

A: Alkyl halide gives elimination reactions when they react with a strong base. The E2 elimination…

Q: Br, Br HBr (xs)

A: SN1 type mechanism  follow.