3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents and intermediates.

Q: NO2 NH2 Br NO2 НООС b. NO2

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Q: O CH3CCH₂CH₂CH3 NaBH4/CH3OH

A: NaBH4 acts as a reducing agent by providing H- ion . It reduces Aldehyde into a primary alcohol and…

Q: Complete the reaction by identifying the major product/s of the reaction:

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Q: ОН

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Q: Complete the mechanism below with the missing structure and arrows. Also identify any acids, bases,…

A: Electrophile is a substance which carry positive charge and nucleophile is a substance which carry…

Q: Design a synthesis that would lead to the formation of the desired product. Please provide arrow…

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Q: Complete the following transformation and provide the detailed steps

A: Aldehyde is protected using a protecting group and another aldehydic group is reduced to alcohol…

Q: The compound shown here is highly unreactive under conditions that favor E2 reactions. Explain why.…

A: Reactions can have either substitution type of mechanism or an elimination type of mechanism. In a…

Q: Он CN

A: This conversion can be done in 3 steps: 1. Conversion of cyclohexene to cyclohexanol, 2. Conversion…

Q: Please

A: We will write all the intermidiate

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: Please provide a synthetic route for this molecule Br

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Q: Supply synthetic routes to the following molecules using the indicated starting materials

A: The synthetic route for preparation of 2-hexanol is as follows,

Q: At which position in the final product is there an ethyl attached?

A: Given that : We have to identify the position of the ethyl group in the final product :

Q: I need a detailed reaction mechanism of this synthesis

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Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Supply the reagent for the…

A: The given reaction is: To identify the suitable reagent.

Q: Q. Can anyone please show me the details steps involved in the retrosynthesis of the target…

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Q: Can you help answer this problem and elaborate the steps clearly and show any reagent and…

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

Q: Please show the complete steps as well as arrowing pushing mechanisms for the following reaction.

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Q: Hello, can you write the explicit formulas of A, B, C and D in the synthesis below?

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Q: 2.) Design a reasonable synthesis for the following transformation. В.

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Q: Using the attached molecule and synthesis, please redraw the molecule showing the stereochemistry…

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Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

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Q: b) A key piece in the synthesis is the molecule below. Provide a reaction that makes this piece that…

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Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: provide the mechanism and reagents to perform the reaction. Br Но

A: To provide the mechanism and reagents for the given reaction

Q: Please clearly draw the overall reaction taking place between methyl salicylate and sodium…

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Q: Construct a three‑step synthesis of 1,2‑epoxycyclopentane from cyclopentanol by dragging the…

A:

Q: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

A: Show a detailed mechanism (using arrows) for the nucleophilic substitution reaction that would take…

Q: Please draw the retrosynthetic analysis by drawing the immediate precursors to the final product.…

A: In accordance with the Markovnikov rule, the anionic part of the attacking reagent will go to that…

Q: Provide mechanism with curved arrows for Part B: Synthesis of benzil

A: PhC(=O)-CH(IH)-Ph on oxidation with HNO3 gives Ph-C(=O)-C(=O)-Ph which is called benzil.  At first…

Q: Propose an efficient synthesis for the ff. transformations: b

A: a) Transformation 1 -

Q: to

A: This synthesis involves Michael addition, Aldol condensation, dehydration, hydrolysis and…

Q: Cyanohydrin formation is useful because of the further chemistry that can be carried out on

A: C=O group is called carbonyl group  Aldehyde and ketone both are combinedly called carbonyl…

Q: so, Cl, H,SO, AICI,

A: The reactant, benzene is treated with SO3/H2SO4 first and then Cl2/AlCl3.  We have to predict the…

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: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Step-1 : 3-bromo-2-methylbutan-2-ol formation Step-2 : Epoxide formation Step-3 :…

Q: H,C-H,C-H2C-C C-H 2. HC H.

A: Terminal hydrogen of alkyne acts as acidic proton  Thus NaNH2  acts as base and carryout acid base…

Q: B. Give a reasonable synthesis pathway for the transformation below. You may use any organic and…

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Q: Please rovide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A: Given that,

Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: ZEU-UEU-UEZ

A: The Diels–Alder reaction is a chemical reaction that occurs when a conjugated diene reacts with a…

Q: here would you cut during retrosynthesis for the following molecule 4 1l ansuuers

A: Given target molecule is beta hydroxy ketone , which is product of aldol condensation reaction.

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: CH,0-P-8 OCH, CH;0O, NaOCH3 H. OCH3 + CH,0 OCH3 CH;OH CH;0 CH;0

A: This is an example of Wittig-Horner reaction

Q: Chemistry Design a reasonable synthesis for the following transformation. E.

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Q: NO2

A: The organic reaction takes place in many steps. These steps involve the use of various reagents.