Part B. Target Required Starting Materials: HN OHC CH,CI CH2CI and CHO and ammonia HN

Q: Identify the reagents appropriate for each step in the following synthesis. Be sure to answer all…

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Q: Provide the missing products in the reaction sequence shown below. You need to show the molecule…

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Q: Et dl LIOH H2 NO H Et 401

A: We have been asked to predict the mechanism for the given reaction. We have been given hydroxylamine…

Q: H. 1. NABH4 2. Neutralizing work-up

A: Here a reaction is given .For this reaction reagents and products are given.We have to draw the…

Q: 1. Show a detailed mechanism for the following reaction. 1. Cl2, NaOH HO, 2. H3O*

A: Haloform reaction :- Formation of carboxylic acid from Ketone in presence of Halide ( Chlorine ,…

Q: Specify the reagent you would use in each step of the following synthesis: step 1 step 2 Reagents…

A: The question is based on the concepts of Organic reactions. we have been given cyclopentanone. we…

Q: Product(s) (1) MeMgCl, Etz0 (solvent) Ph' Me (2) HCl(aq) "work-up"

A: We have to draw the product of the reaction below, including step by step reaction mechanism with…

Q: Please provide a way to synthesize the target compound using the reagents given below once Target…

A: The conversion reaction is given in the following step.

Q: 6. A synthesis of a molecule being explored as an antidepressant drug (J. Org. Chem 2012) utilized…

A: AlCl3---> It is a lewis acid. it accepts the electron. CH2=CH2 (Ethene): It acts as a nucleophile…

Q: The major product for the following reaction is H. 2CH3OH H+ OCH3 OCH3 OCH3 H H. OCH3 HO. OCH3 OCH3…

A: Aldehyde reacts with alcohol in the presence of acid forms an unstable product hemiacetal which…

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the phthalhydrazide…

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Q: The following alkyl azide (R-N3) can be synthesized in two synthetic steps. Propose a two step…

A: Both the steps occurs via Sn2 mechanism.  In 1st reaction, OH is not a good leaving group. In…

Q: Show the reagents and intermediate products in the following multi-step synthesis. CH3 а) CН — -H…

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Q: Be sure to answer all parts. Predict the product of the following reaction and then draw a stepwise…

A: Here, in the given reaction, Bromide ion substitutes the -OH group and leads to formation of Alkyl…

Q: Draw the major organic product of the reaction, which has the molecular formula C,H,N. Select Draw…

A: For the given molecule The following is the major organic product::---->

Q: Show a possible mechanism for the following reaction 1) LAH (xs) 2) H3O* 3 MeOH

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Q: Complete the following multistep syntheses by showing the major intermediate products and the…

A: We have find out the reagents

Q: Part 2: Simple Reactions Draw the structure resulting from the following HC1 + HOCH₂CH₂OH CH₂OH Dess…

A: We have to show the major organic products.       N.B. According to the company guidelines, we have…

Q: Devise a 4-step synthesis of the product from the starting material. CH3 1. reagent 1 2. reagent 2…

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Q: GS Q5 Show all missing reagents and intermediates in the reaction sequence below. Put the…

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Q: What is the product of the following sequence of reactions? 2Li Cul pentane ether ether 1. m 3. er…

A: We have been asked to find the product by following given sequence of reactions. This reaction…

Q: OH

A: To prepare benzyl phenyl ether, firstly cover phenol in to phenoxide ion.

Q: Select the major product of the reaction sequence below. OH NHČCH, NHCHCH, NHCH,CH, NHCHCH, NHCH,CH,…

A: Step 1: Fridel Craft's Acylation at the para position.Step 2: Reduction of amide and ketone group to…

Q: Find the major product from the following reaction sequence: 1. PCIS OH 2. CH;NH2 3. LİAIH4 4. Н.О+

A: In the given reaction the acetic acid reacts with phosphorus pentachloride to form acid chloride.

Q: redict the correct final product of the following sequence of reactions. CN 1) PhMgBr 2) H2O NH он…

A: Applying nucleophilic addition reaction on nitrile group to produce corresponding carbonyl group.

Q: Propose an efficient multistep synthesis for the transformation shown below. There is no need to…

A: This compound can be synthesized in 4 steps. Step-1 is the selective reduction of keto group of…

Q: NaOH -ċ-Br 50°C

A: See answer below

Q: 3) write a detailed mechanism for the following reaction: Br hv light + HBr + Br2

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Q: Which synthetic route represents the best method for generating the target molecule below? Route A…

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Q: Which compound would be the product of the reaction sequence shown below? MgBr 2. H30*/H20 3. РСС 4.…

A: RMgBr is a grignard reagent and it attacks the carbon attached to double bonded Oxygen atom and join…

Q: Propose a sequence of two reactions that transform the starting material into the final product.…

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Q: estion 6 Select the major product of the reaction sequence below. CI CHNH2 COCNH, 1. (COCI)2 CO,H 2.…

A: In this question, we will Select the correct major product for this reaction.  You can see details…

Q: 6. A synthesis of a molecule being explored as an antidepressant drug (J. Org. Chem 2012) utilized…

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Q: Propose a sequence of two reactions that transform the starting material into the final product.…

A: Reagent 1. KOtBu(potassium tertiary butoxide), t-BuOH(tert-butanol as a solvent) 2. M-CPBA in…

Q: 1. CH2=CHLI 2. НзО*

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. CI 1. CH3MGBR (excess) 2. H20

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Q: H. OH

A: Here, the transformation of Benzaldehyde to Benzyl Alcohol is done. The appropriate reagent is…

Q: Propose a synthesis for each of the Target Molecules below. You may use any reagents you wish, but…

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Q: ОН Na2Cr207 H2SO4, H2O

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Q: Find the major product from the following reaction sequence: HO 1. НО+, но ? 2. CH;MgBr, Et.O…

A: Applying concept of protecting groups of ketone and nucleophilic attack by RMgBr followed by acidic…

Q: Specify the reagent you would use in each step of the following synthesis: CI step 1 step 2 H.…

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Q: 3. Propose a mechanism for the following reaction sequence. Et 1. BuLi, 2 moles 2. CH3CH2Br Ph

A: The reaction proceeds with a nucleophilic addition elimination reaction mechanism at the carbonyl…

Q: Devise a synthesis for the following transformation. SM = starting material. TM = target molecule Br…

A: We have to perform the transformation:

Q: 1. CH3CH2MgBr 2. НзО*

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Q: Review the reactions below. Select the reagent needed to carry out each reaction as shown. он I. он…

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Q: 3. Propose a synthesis of the target molecule using the starting material below. You may use any…

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Q: What is the final product of the multi-step synthesis sequence of reactions shown? NaNH, NH, LINH;…

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

Q: Propose a mechanism for the reaction below: 12 (excess) OH™ + CHI3

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Q: Predict the product and draw a stepwise mechanism for the following reaction: Part 1: Br HBr HO view…

A: The reaction described here is a acid catalysed dehydrtion followed by nucleophilic attack on…

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.