Draw the major product of the following reaction a). Remember to include the stereochemistry of the methyl groups. HCltrace) OH b). HCltrace) MeOH ||

Q: b. Draw the FULL electron-pushing mechanism for the reaction depicted including ALL intermediates…

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Q: CHO

A: The given reaction Diels–Alder reaction . In this reaction one conjugated diene and dienophile react…

Q: Draw a major organic product for the reaction shown. Clearly show stereochemistry by drawing one…

A: A substitution reaction which involves the substitution of two atoms of a molecule to the different…

Q: From each pair, select the stronger nucleophile. Q.) CH3OCH3 or CH3SCH3

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Q: Show how each alkene can be synthesized by a Wittig reaction

A: Wittig reaction is an organic synthesis reaction which is used to synthesize alkene by reacting a…

Q: In the lab, a student desires to obtain compound A but instead always getting compound B as the…

A: It is an electrophilic aromatic substitution reaction.

Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

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Q: H

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Q: Br „CH3 CH3CH2OH H3C"

A: Organic reaction mechanisms

Q: For each reaction, draw the complete mechanism and the major organic product(s), paying attention to…

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Q: hv > ? Major product *product (Stereochemistry (ii) Minor it st be denicted)

A: General  saturated  Ketone  undergo following  reactionsis presence  of light hv

Q: CN NaOH HO H20 NC

A: Solution :         NaOH and water used as a reagent.NaOH is a base that is used to abstract…

Q: 1. Draw the structure of (4S)-1-bromo-4-methylhexane a. Draw the substitution product that would…

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Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

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Q: Draw the major organic product of the reaction. Indicate the stereochemistry via wedge-and-dash…

A: • Nucleophillic substitution SN2 reaction has the           following charactershics :-i if follow…

Q: Explain how and why the reaction below results in the observed regiochemistry and/or…

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Q: a-Draw out detailed mechanisms for each reaction including electron pushing arrows, intermediates…

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Q: Which reagent(s) complete this transformation?

A: .When secondary alcohol  react with  oxidising agent  then convert into ketone . .Reactant name is 2…

Q: Major

A: We have to write the final product.

Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: :ÇI: CH3 + KOTBU H,C ČH3

A: Here, strong base/nucleophile is present, so there is a possibility of substitution as well as…

Q: Alkyl substituents are: Select one: O a. Strong, meta directors O b. Strong, ortho/para directors…

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Q: Consider the nucleophilic substitution reaction shown here. Based on the stereochemistry, does it…

A: Nucleophilic substitution reaction is the kind of reaction where electron-rich nucleophile attacks…

Q: Why do carbocation rearrangements occur? Choose all that apply. Ring strain can be reduced. They…

A: Carbocation rearrangements are the organic reactions in which the movement of an unstable…

Q: A carbocation is a good a) electrophile b) nucleophile c) neither O a O b

A: In this question, we will see that the carbocation is a good Electrophile or Nucleophile.  You can…

Q: or each addition route of the reaction, draw the structure(s) of the major product(s), including…

A: Answer of the question given below,

Q: 4) Draw all mechanistic steps (initiation, propagation, termination) for the following…

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Q: Draw the major product of this reaction. Include stereochemistry if applicable. Ignore byproducts.

A: Given : structure of reactant.  This is SN2 reaction. Removal of cl- and attack of Nucleophile will…

Q: Draw all possible products in the following reaction and circle the most stable product. Br КОН ELOH

A: In this question, we will draw all products for this reaction and the circle the most stable…

Q: Show how a 1,2-shift forms a more stable carbocation from each intermediate.

A: The shift occurs in ionic species .and the shift males the carbocation more stable.  In 1st…

Q: ne major product?

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Q: он CN

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Q: Draw the major product of this reaction. Include any relevant stereochemistry. Ignore inorganic…

A: Phosphonium ylides are used in the Wittig reaction, a method used to convert ketones and especially…

Q: For each pair of reactants (A-C) draw all possible E2 products, label each as a mono, di, tri, or…

A: When an alkyl halide reacts with a strong base, the reactants can undergo two mechanisms. The…

Q: Synthesis F Please Include the reagent and intermediate as well as the Meta direction OH acyclic…

A: The desired product can be made by using Diels-Alder reaction. The detailed mechanism is in the next…

Q: Br or Br Br C or CI || CI or CI ||

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Q: Draw the major intermediate and product of the reaction between (2E)-4-methylhex-2-ene and Br, in…

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Q: Rank the following carbocations from most stable to least stable. +) +) A B C

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Q: Draw an alkyl bromide with proper stereochemistry that can be used to synthesize the given alkene as…

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Q: How would I use Gabriel synthesis here?

A: Gabriel synthesis:

Q: Draw the major product of the following reaction. Be sure to include stereochemistry if applicable.…

A:

Q: In the given condensed formula, I understand that there will be a carbocation rearrangement due to…

A: The E1 mechanism of conversion of secondary alcohol to alkene is given in step two.

Q: Draw a curly arrow mechanism to clearly describe why the following reaction gives a trans dibromo…

A: Reaction of alkenes with bromine results in the formation of vicinal dibromides i.e. 1,2-dibromides.…

Q: A)

A: Here we have to prepare the following given compounds from alkyl halide containing four carbon atom…

Q: HCI b.

A: First reaction involve allyl carbocation intermediate and second reaction is diels alder reaction

Q: CH3 CH, H3C-¢* + :Br: H,C Br : CH3 CH,

A: The movement of electrons are shown by curved arrows. There are two types of arrows to show the…

Q: ROOR

A: Here the reagent is an alkene and it is being treated with ROOR.

Q: What

A: We will write the product

Q: This addition of HBr to (Z)-2-bromobut-2-ene takes place regioselectively, with the Br…

A: a) A detailed mechanism for the reaction, including initiation and propagation steps has to be…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.