c) Show a reaction that would have Brz adding across the double bond of an alkene, and draw the bromonium ion intermediate. Then show why the reaction results in anti addition of the bromines.

Q: What are the products for each of these? What's the whole mechanism for B?

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Q: First, draw the structure of the alkyl bromide that will ONLY give the alkene shown in an…

A: Elimination reaction are those reaction where functional group is lost to form unsaturated compound…

Q: Does either reaction produce multiple stereoisometric products? Which reaction occurs fastest? Does…

A: The reactions that involve the elimination of the leaving group belongs to a molecule by the…

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: Provide the step-wise mechanism for the ffg.. Draw the intermediate/s involved in each rxn. This…

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Q: Draw curved arrows to show the movement of electrons in this step of the mechanism.

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Q: Select the electrophile (A, B, or C) in the following reaction step.

A: Electrophile is an electron deficient species or a neutral compound having an incomplete octet or…

Q: What are the errors in the following answer?  Note: If the product has ortho or para substitution,…

A: In a substitution reaction, one substituent in a chemical compound is replaced by another.  When a…

Q: The above reaction proceeds to yield only a single product. Draw the structure(s) of the…

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Q: For the reaction shown, draw the product of one mole of reagent adding across the triple bond, and…

A: In the given reaction Product A and Product B are to be determined. This is an addition reaction and…

Q: What are the compounds X,Y and Z in the given reaction sequence ?

A: When potassium dichromate react with the Silver nitrate it gives the silver chromate as a insoluble…

Q: The attached reaction does not afford the major product that is given.Explain why this is so, and…

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Q: Help Please☺ 1 Which Substrate reacts more rapidly? CI a) or or Br

A: Organic chemistry is branch of chemistry in which reactant react to form organic products.

Q: What is Lucas reagent made of? explain.

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Q: он Br

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Q: Use curved arrows to denote electron flow in this first step. Draw both possible carbocation…

A: In the given question an example of hydrohalogenation reaction is provided. Hydrohalogenation…

Q: Why energy required to reach transition state is lower in active site? And not Lowe in any other…

A: In a particular reaction, the minimum amount of kinetic energy required by the reactant molecule to…

Q: draw the step one product and draw curved arrows to show the nucleophilic addition step.

A: To provide the arrow mechanism for the first step of the Fischer esterification reaction and the…

Q: For the reaction shown, choose the most likely reaction pathway and draw the organic product.

A: This reaction can happen by Nucleophilic substitution reaction .  Here azide ion as the nucleophile…

Q: Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.

A: Sequence :-  Protonation of alkene Carbocation rearrangement Attack of methanol as nucleophile…

Q: Drawing the Products of an SN1 Reaction Label the nucleophile and leaving group, and draw the…

A: the nucleophile and leaving group

Q: NaH

A: Aldol condensation : In presence of base when ketones or aldehyde reacts to another keto or aldehyde…

Q: Please draw the missing product and the arrow pushing mechanism. Please identify all charged atoms…

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

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Q: what is the mechanism of this reaction? b) is this the only product formed, meaning is the reaction…

A: The reaction follows electrophilic substitution mechanism. When a benzene ring has two substituent…

Q: Explain why alkylation of an α-carbon works best if the alkyl halide used in the reaction is a…

A: The alkylation reaction of an α-carbon depends on the R-X (alkyl halide) used in the reaction. The…

Q: Brz. FeBr NaOMe

A: Organic Transformation and Mechanism

Q: Use curved arrows to denote electron flow in this first step. Draw both possible carbocation…

A: When alkene is treated with Hydrogen halide, then addition is take place According to Markonikove's…

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: Follow the curved arrows and draw the products of the following reaction.

A: Since the lone pair of O from the diol molecule is attacking and forming the product

Q: Draw the mechanism for each of the following reaction. Show all steps in the reaction, the…

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

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Q: Fill in the appropriate reagent or starting material in each of the attached reaction.

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Q: Which is a correct mechanism step in the formation of an acetal?

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Q: Write the correct mechanism and major product for a), and indicate the reagent needed for b) to…

A: Two question based on alkenes, which are to be accomplished.

Q: a. Which is a stronger base: RO- or RS-? b. Which is a better nucleophile in an aqueous solution? c.…

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Q: What is the complete mechanism for this F!she rxn?

A: When carboxylic acid is treated with alcohol in the presence of mineral acid, generally H2SO4, we…

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

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Q: Draw a stepwise mechanism for the attached reaction. (Hint: Conjugateaddition can occur with…

A: Nucleophilic Conjugate addition reaction: The reaction will take place when In  α-β unsaturated…

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: Can you show step by step of this missing reagent and show the synthetic intermediate?

A: Selective reduction of ester in present of ketone is done by NaBH4. We protect the ketone so that…

Q: Draw the product of the attached reaction:

A: In this reaction, OH- acts like base and it abstract the more acidic hydrogen and then negative…

Q: Show complete mechanism including transition state for an SN, reaction of a specific chiral alkyl…

A: Hi! Since there are multiple questions posted. We are answering first question. If you need further…

Q: For the following reaction step, indicate which pattern of arrow pushing it represents. A…

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Q: Add missing reagent(s) while also showing stereochemistry of the product of the second reaction.

A: In this question we have to complete the given organic reaction.

Q: Can you please check if the reagent and intermediate are correct as well as the Meta direction

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Find the diene and dienophile for the following product (retrosynthesis): ? + ? B B

A: Retrosynthesis: When Reaction  is carried out from product to Reactant side Then reaction is called…

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.