OEt OEt OEt

Q: Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the…

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Q: Provide reagents for the first transformation

A: First, we have to convert Alcohol to Acid followed by Acid chloride.  Then Acid chloride with…

Q: Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the…

A: A Russian chemist “Vladimir Markovnikov” formulated a rule to identify the outcome of the some…

Q: Show the electron-flow mechanism of the chosen synthetic schemes. This involves predicting major and…

A: Benzene Sulfonic Acid to Phenol

Q: Give the appropriate reagents for each of the following synthetic conversions......?

A: Reaction 1 , 2,

Q: Devise a synthetic strategy to complete the following transformation.

A: GIVEN:-

Q: Complete the synthesis of the target molecules below (on the left) from the starting material (on…

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Q: Find a synthesis route for the transformation below Br

A: In this question, we will synthesized the final organic product from the starting material by using…

Q: OCH3 only source of carbon

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Q: Use curved arrows to show the movement of electrons in the following E2 mechanism. Draw the…

A: E2 mechanism is a concerted mechanism.

Q: What is the missing product or reagent needed to complete these reactions?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the…

A: Here, we have to construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene.…

Q: Propose an efficient synthesis for the transformation below. Step 1 .Step 2

A: In this question, we want to identify all two step Reagent ( step-1 and step-1 ) for this given…

Q: Step 1 CI Benzoic Acid Thionyl Chloride Benzoyl Chloride Step 2 "y" NH2 HNH Benzoyl Chloride…

A: The process of conversion of benzoic acid into aniline involves the following steps: Step 1:…

Q: Devise a synthetic strategy to complete the following transformation. но

A: Retrosynthetic analysis is that where we have try to generate target molecule from the ultimate…

Q: In the reaction series below, write down the appropriate reagents that can be used where there are…

A: The reaction  is completed in the diagram below.

Q: Propose an efficient synthesis for the transformation below (enter the appropriate code from the…

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Q: Choose the starting materials needed to complete this Robinson annulation reaction. Assume an acidic…

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Q: Use curved arrows to show the movement of electrons in the following E2 mechanism. Draw the…

A: E2 mechanism is a concerted mechanism.

Q: write the missing reagents and solvents over the arrows. Some transformation require multiple steps.…

A: Terminal alkynes (1-alkyne) upon treated with butyllithium (BuLi) gives "lithiumacetylide" is…

Q: What are the best reagents to perform this transformation? ? ОН Он н РСС, CH2CI2 CrO3, H30, acetone…

A: The oxidation of alcohols in the presence of a strong oxidizing agent first, forms a carbonyl…

Q: Complete the following synthetic transformation by selecting from the list of reagents below. Each…

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Q: Add curved arrows to the structures shown below in order to complete the mechanism. OCH3 OCH3 НА OH…

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Q: Forward synthesis of 1-pentyne: Na*H- H-C C: CI H-C=C-H + H, target compound Now it's your turn to…

A: Addition of HOCl to alkene gives halohydrin Reduction of alkyne in the presence of Lindlar catalyst…

Q: Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an…

A: a) In SN1 reactions, the intermediate formed is carbocation. When alcohols reacts with HX (where HX…

Q: Select the best reagents to affect the transformation below. ?

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Q: Choose the best reagent to complete this reaction. Assume an acidic work up. NH2 NH2

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Q: Shown below is the conversion of pivaldehyde to tert-butyl benzoate. Fill in the best reagents to…

A: Given: To find the best reagents for the synthesis of the given product,

Q: Fill in the reagents or synthetic intermediates in the following scheme. 1) NaOEt / EIOH 2) Но

A: Step 1 : Bromination of cyclohexane under light. Step 2: E2 elimination of cyclohexyl bromide. Step…

Q: Which pair of reactants is most likely to undergo an S№2 reaction? CH3CO₂Na + (CH3)2CHCH₂CH₂CH₂Br at…

A: The answer is- (a)

Q: Choose the best reagents to complete the reaction shown below.

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Q: 1. Provide reagents for the first transformation of the synthetic sequence shown below. Draw the…

A: In presence of strong oxidising agent primary alcohol transforms into carboxylic acid via aldehyde…

Q: 3. For the following synthetic schemes, please draw the product(s) to the right of the arrow. 1.…

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Q: Fill in the appropriate reagents to achieve the synthetic transformation shown below. Note: If one…

A: Steps involved to achieve the synthetic transformation of the given reaction can be shown as…

Q: Propose a sequence of synthetic steps that would efficiently accomplish the conversion shown below.…

A: Cyclopentane undergo photolytic bromination to give cyclopentyl bromide. On heating with NaNH2/liq.…

Q: What is the expected product of the reaction sequence shown? Assume only the expected major product…

A: the reaction can be shown as:

Q: This compound was made from a conjugated enone using a multi-step synthesis that included a direct…

A: The enone can give an addition reaction at C=C and C=O. The addition reaction at C=O is known as a…

Q: Use curved arrows to show the movement of electrons in the following E2 mechanism. Draw the…

A: The movement of electrons in the following E2 mechanism has to be shown The structure of the…

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

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Q: OH so,H So, Na* O Na* NaOH NaOH H,0* H,0 350°

A: Given,  Benzene Sulfonic Acid to Phenol

Q: and ANY COMPOUND up to 2 carbons

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Q: .From the two synthetic routes shown below which one would be the best route for the desired…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: HO3S Select to Draw CI CH3C(=0)CI Select to Draw AICI3

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Q: 10. Propose a synthetic scheme to accomplish the following transformation. NO2 ОН

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Q: Based on your knowledge in biological chemistry reaction in biomolecules, what do you think is the…

A: Given reaction is :  Based on your knowledge in biological chemistry reaction in biomolecules, what…

Q: In each case below select the synthetic procedure that could be used to carry out the transformation…

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Q: Make an electron-flow-mechanism for this synthetic scheme. This involves predicting major and…

A: By electrophilic substitution reaction benzene is converted to benzene sulphonic acid

Q: CH3 CH2BR NBS hv

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Q: но, b) H

A: