Complete the following synthesis by adding the missing reagents NWOHICH3CH2Br NaOHICHOCHOCHB NaH/CH3CH2CI H2/Pt H2SO4. HgSO4, H2O Na/NH3 H2/lindar Pd NaNH2 NaH/CH3CH2CH2Br

Q: НО, Me N OH NH2 НО, Me `N ОН ОН

A: To propose a synthetic route for the given target molecule from the given starting material

Q: Give Step by step solution

A: Step 1: Step 2: Step 3: Step 4:

Q: Using benzene as starting material, devise a synthesis for the target compound in 3 steps by…

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Q: Step 3: If excess alcohol is present in the hemiacetal, the hemiacetal can be further converted to…

A: Answer:Hemiacetal is a compound in which one OH and one OR group is connected to the carbon atom…

Q: Draw the missing organic structures or select the missing reagents in the following multistep…

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Q: Synthethic

A: 1- EtOH, H+ ( Formation of ester bond ) 2- H2, Pd(C) [ removing of protecting group )  3- K2Cr2O7,…

Q: 1. 98% H2SO4 Ме OMe Br- -78 °C 2. Li e ČO,Me OMe -78 °C-rt, THF

A: Robinson annulation followed by Quasi-favorskii reaction will give the desired product.

Q: 1) [H*), HỌ 2) NaNH, 3) Etl 4) H3O+ 1) [H*]. HỌ 2) Etl 4) H30* 1) [H*]. HỌ 2) NaNH, 3) Etl 1) [H*].…

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Q: Provide reagents/conditions to accomplish the following syntheses. Several steps are required in…

A: In this question, we will provide reagents/conditions ( conditions like using solvent or heating )…

Q: Provide a step by step mechanism for the following transformation. NH2 N2* HCI, NaNO2 H20

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Q: For each of the following, provide the product or reagent as necessary. H20 NABH, + Hg(OAc)2 ELOH 1)…

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Q: What are the best reagents to complete this transformation? OH BH3 / THF followed by H2O2/ - OH…

A: Answer:

Q: 2. Complete the following reaction. Show the intermediate, and propose a mechanism for the second…

A: This is an example of Hoffmann elimination reaction. In this reaction proton is abstracted from the…

Q: 1. ВНз THF 2. H202 N2OH CH, H,C- -CH,

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Q: Complete the following benzylic position reaction diagram by filling in the missing reagents. OH Br…

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Q: 4. Both the Markovnikov and anti-Markovnikov hydration of alkynes proceed through an enol…

A: Enols are hydrolysed in presence of either acid or base to give corresponding ketone or aldehyde as…

Q: H3O*, Br₂ NaOEt. wwwmmmm EtOH H3O+ NaOH, H2O

A: Step wise reaction explained:

Q: Select the best reagents to produce the product shown as the major or exclusive product. OH O…

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Q: b) Synthesize the following product starting with phenol (hydroxybenzene). NO₂ OH HO. phenol

A: The question is based on organic synthesis. we need to synthesize the product based on Reactant…

Q: 1. Fill in the blanks with the MAJOR organic product in the following electrophilic aromatic…

A: Since you have posted multiple subpart questions, the answer for first three subpart question is…

Q: In the below reaction, the starting material functional group is [Select] . This functional group,…

A: The atom or group of atoms attached to an organic compound that decides the characteristics of the…

Q: НО- O H CH₂ OCH

A: -> Hydroboration oxidation of alkene give antimorkovnikov addition of H2O overall and form…

Q: 1 what is the iupac name for the following a a 1 b 2 12 Show the williamson ether synthesis reaction…

A: Dear student, as an expert we are only allowed to answer one question at a time and 3 questions at a…

Q: Provide an arrow pushing mechanism for the following reaction. Include protons and each step clearly…

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Q: Complete each reaction scheme below with the starting material required to give the product shown as…

A: Three membered rings formed by two carbon and one oxygen atom is known as epoxide ring. The…

Q: HO ??? LOH

A: The given conversion is from propanol to butanoic acid . Propanol ----------> Butanoic acid .

Q: Which of these compounds would exist primarily in an enol form? OA. OB. OC. D. OE.

A: Keto enol tautomerism is a type of structural isomerism. A chemical equilibrium between the keto and…

Q: What reagent(s) will accomplish this conversion? EtLi followed by an acid wash O EtzSiCI followed by…

A: the given reaction is 1,4-addition to the alpha beta unsaturated ketone.  where the nucleophile is…

Q: 4) Synthesize the following molecule using the indicated starting material, showing all reagents…

A: Solution: We know the mannich reaction in which carbonyl compound with Alpha hydrogen are treated…

Q: f. g. h. a a a= 6 = Xe Br2 CH3CH₂OH H₂SO4 H₂ Pd/C

A: The given reaction is an example of anti- addition reaction of bromine on olefins . In this type of…

Q: Select the reagents that will allow the following transformation(s) to occur. -H ? 1) NaOH 2) propyl…

A: The transformation reaction from propyne (also known as methyl acetylene) to hex-2-yne involves…

Q: Determine why these reagents wouldn't work to form the product given using the same starting…

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Q: 1) LiAlH4; ) H3O+ will do which of the following reactions?     3-Phenyl-butanoic acid  →…

A: The reagent is i) LiAlH4; ii) H3O+.

Q: OH Provide a reasonable synthesis of 1-cyclohexyl-1-ethanol starting from cyclohexanol. OH

A: The objective of this question is to provide a reasonable synthesis of 1-cyclohexyl-1-ethanol…

Q: Propose a detailed mechanism for the reaction below. HNO3 H₂SO4 NO₂

A: The nitration of benzene  is typically carried out in the presence of a mixture of concentrated…

Q: Br NH2 NANH2 NaBr

A: The reaction of bromobenzene with sodium amide results in the generation of aniline and sodium…

Q: Select the best reagents to produce the product shown as the major or exclusive product. OH O…

A: A reaction is given in the question. We have to find the reagent from the options for which the…

Q: OH 2-lodobenzoic acid K₂S208 H₂SO4 OH OSO3H OH diphenyliodonium-2-Carboxylate benzyne

A: Oxidation of iodine by peroxydisulfuric acidAromatic electrophilic substitutionBenzyne formation

Q: rank these from least to most reactive in nucleophilic acyl substitution with a nucleophile…

A: CH3COOC2H5CH3COONaCH3COClCH3CONH2

Q: Determine the intermediates and product(s) for the following synthesis sequence. O d ملی میں LDA HD…

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: 1. Complete the following transformation, show step-by-step scheme "iy" H H H AND

A: The above given formation of products from the provided starting materials can be carried out in…

Q: Categorize propose reagents to carry out the multi-step synthesis according to the retrosynthetic…

A: The question is based on the concept of organic synthesis. we have to form the product from the…

Q: u. H20 H2SO4 V. HBr W. H2 Pd/C

A: Alkenes are hydrocarbons having at least double bond in their structure. Alkene undergoes hydration,…

Q: Fill In Missing reagents and products in the cmpty boxes. Br. HOOH NH2

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Q: H2SO4 Он

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Q: CH3 NHCH3 CH3 CI CH,NH2 triethylamine

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Q: Provide a detailed, stepwise mechanism for the following reaction. Br NH2 + NaNH, + NaBr

A: For given question there is need to determine mechanism of bromobenzene and NaNH2

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.