Supply the missing reagents, intermediates, and final product in the following synthesis. OH A 1. B 2. NH,CI TBDMS TBDMS Bu,NOFO F H,0 1. E H2SO4 2. NH,CI Но

Q: Supply the missing compounds in the following synthesis scheme. 1. NaNH2 (3 equiv) H CCI4 Br2 1.…

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Q: What reagents would you use to carry out the following reaction? (A) H₂ / Pt (B) (C) (D)…

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Q: 1) NaBH,/ CH,0н 2) H2O HN

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Q: 1. 2. 3. Br NO₂ H₂SO4 Br₂ FeBr3 AICI3

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Q: hno3/ NH2 NO2 h2so4 3. ? 4. ? ALCL3/CH3CL HO 1.. Li 2. Gul NaSH, DMSO LDA/DIPA CH3Br O3/DMS heat NBS…

A: Given

Q: Every transformation can be completed in one 'synthetic ste added sequentially, ex. "1. BH3, THF; 2.…

A: Given : We have to write the reagent for the following.

Q: What would be the major product of the following reaction sequence? H+ ? CH3OH OCH OH OH OH он OCH3…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: BOH)2 Pd(PPH3)4 Br K2CO3

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Q: Cl Br А D E B

A: SN1 and E1 reactions is that SN1 reactions are substitution reactions whereas E1 reactions are…

Q: 1) Оз 2) H20

A: The answer to the given question is as follows........ Ozonolysis of alkyne give two carboxylic…

Q: a good leaving group such as iodide. .CO₂H base НО 15 17 co Mecarmis SN2 ميكا تكيه ها التفاعل + TM3…

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Q: 4. Draw the final major product(s) for each multistep synthesis reaction. H30* -OMe H3PO4 Jones…

A: 4a. Ketal deprotection using acid. b. hydration of cyclohexene. oxidation of cyclohexanol.…

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: Select the reagent that you would use to convert an alkene to an epoxide. mCPBA 03, then DMS…

A: The epoxide is a cyclic ether with a ring structure consisting of three atoms that somehow form an…

Q: A student attempted to synthesize an epoxide according to the reaction scheme shown here, but no…

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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: 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: HO Br2 (1 equiv) 0° C

A: The above reaction proceeds through a free radical mechanism as follows:

Q: 5. Propose a synthetic pathway for molecule X to molecule Y using the reagents boxed below. Note…

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Q: 4. Propose a mechanism for the SUBSTITUTION reaction below: HINT AICI, is an ELECTROPHILE. H3C ÇH3…

A: The given reaction is a Friedel - Crafts alkylation reaction. In this reaction alkylation of…

Q: Enio bns 200 HO HO ONLY

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Q: 2. Assume all reactions add the reagent once. Will the following reactions produce the major product…

A: Electrophilic addition reaction will favour at that position where electron density is high . Note:…

Q: Draw the final product of this series of reactions. Br 1. 1 equivalent of KOtBu 2. MCPBA 3. H3O*/H2O

A: The reaction given is,

Q: Propose reactions to synthesize each compound above. (Note: If the reaction procedure is not your…

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Q: K (Most stable intermediate) CC, dil. H,SO, M N (Product) (Minor E1 product)

A: In this reaction first π bond breaks and H+ attack on anion and carbocation is formed which is 2°…

Q: In the following synthesis, there are 5 steps that must be done in the correct order (i.e. Step #1,…

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Q: Rank these nucleophiles from best to worst Na- I -I Best (II)>(1)>(III) worst Best (1)>(III)>(II)…

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: 6. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed…

A: → In above base is weak so it show SN2 reaction.

Q: 4) Draw the major product of the following reactions (hint: watch out carbocation rearrangement): Br…

A: Given reactions are example of F.C. alkylation reaction.

Q: H3O*

A: The given is the acid-catalyzed hydrolysis of alkene. The first step is the nucleophilic attack of…

Q: H3C I NaOH Меон, 82 °C

A: Sodium hydroxide abstract the proton forms carbanion. The formed carbanion forms alkene with…

Q: EIO 1. 2. он OH OE! 3. NO, 5. ???? OEI Remember - can't use simple enolate enol 7. for SN2 type…

A: Note : First do the retro synthesis. Then plan the synthesis.

Q: 38) Complete the following reactions with the proper major products. SO3/H₂SO4 Br2 FeBr3 MeCOCI…

A: Step 1 : Fridel craft acylation. Step 2 : Ortho isomer ( Sulphonation takes place at para position…

Q: Please complete the following synthesis. Br 3 A E B D Brz, hv Br2, DCM HBr, DCM LDA HBr, H2O2 H I F…

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Q: Which starting materlal will result In this product when these reagents are used? Click on a letter…

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Q: show products and mechanism for reaction below: ** O Unel Tommation| (a) Pd(PPH3)4 OMe EtzN (b) 1)…

A: In presence of Pd catalyst,  aryl halide undergo oxidative addition and followed by coupling…

Q: C. Show the product formed in each step of this multi-step synthesis. Br2, H3O+ KOtBu immmmmm NaOH,…

A: The answer is as follows:

Q: 4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones Et,NH…

A: 1. Acetal compound can be deprotected in presence of H3O+ and forms ketone or aldehyde compound.  2.…

Q: Which reaction schemes is best to give the product? HO. NO 2 O The following reaction scheme: CH3…

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Q: What is the best reagent to complete this synthesis? 1) ???? 2) NaCN OH CN A. PBr, B. C. CiSIMe;…

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Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…

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Q: Me „CHO CO2E Me + Ph3Ps .CO2E† Me CH2CI2 Me 0: Me Me 40 °C, 60 min, 89 % (3 steps) Me See the Wittig…

A: Wittig reaction is an organic chemical reaction wherein an aldehyde or a ketone is reacted with a…

Q: Which reaction(s) would occur in the reaction below (substitution, elimination, both, or neither)?…

A: the correct option is:

Q: .CI AICI, 'CI 'CI

A: Ans  Electrophilic substitution reaction takes place

Q: 1. 1eq. Eto /E£OH OEt 2. H30® Dieckman cyclization product ОН Anhydride NH2 1ед. 1eq NaOH O=

A: the detailed mechanism the structure of reactant or product will show below in attach image.

Q: HO OCH3 OCH3

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Q: Reaction C Modify the structure to give the product of reaction C. Draw the counterion. Select Draw…

A: the given molecule is a tertiary amine. We know that tertiary amine has a nitrogen having a lone…

Q: Identify compounds A-G in the following synthesis scheme. Mg(s) A В Et,0 1. 2 2. Н,О, НСІ РСС D Br2…

A: Compounds A-G has to be identified.

Q: Draw the major organic product from the reaction sequence provided: Select Draw Rings More C H. Cl…

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