MCPBA tBu Ph M) (H,SO H,N NABH,CN N) NaOH, H,о Нeat

Q: 1) N-H /H® 2) 3) H20 / HO ZHN NABH3CN

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Q: ミッションX Cl b. / Hol プ れた。 ↓

A: Here we have to synthesize the following given compounds from the given starting materials by…

Q: a) Br (only product) b) I I ( CH₂CHCH₂CHCH₂ C) H₂₂C A Br H₂C CH₂

A: Preparation of molecules given using any alkene:

Q: a) propin b) HO,

A: Organic reaction mechanisms

Q: (а) но (b) -CH3 он (гасemic)

A: In this question, Reactants and Products are given and we used the Reagents to carried out this…

Q: Provide the major organic product of the following reaction. H3CH2C CH2CH3 HNO3, H2SO4

A: The given reaction is electrophilic aromatic substitution reaction. In this reaction nitration is…

Q: Provide the major organic product of the following reaction. CH3CH₂CH₂CH₂CO₂H CH,CH,CH,CH,CHO…

A: Carbonyl or carboxyl group derivatives having alpha-H can react with a base to form an enolate ion…

Q: + CH3NO2 NAOH 1) LDA, THE 2) CH3I EtO OEt 1) NaOEt, E1OH LDA 2) CH3CH2B H30+ H20 A

A:

Q: Please identify major PRODUCT A and major PRODUCT B.

A: We have given the organic reaction and we have to identify major PRODUCT A and major PRODUCT B

Q: OH OH Phph Ph CrO3 H₂SO4 SOCI₂ een H HN(CH,CH3)2

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Q: + CI cat. H* - H₂O cat. H - H₂O HO

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Q: Synthesize the products by drawing out reagents and intermediates along the way.

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: HO. H2SO4. Η ΟΗ Η H+, H₂O ΟΗ 요

A: Aldehydes upon reduction gives alcohols.Diols are used to protect the carbonyl compounds. H2SO4 used…

Q: 41. HNO3, H₂SO4 2. H₂, Pd/C 2_1 C10H15N 1. NaNO2, H₂SO4, H₂O, 0 °C 2. Cu₂0

A: Substituted benzenes upon treatment with concentrated nitric acid and sulfuric acid, undergoes…

Q: 1. LIAIH, OMe 2. acidic workup A HO. B 1. excess MeMgBr (> 10 eq.) OMe но. 2. acidic workup H3O", A…

A:

Q: Provide the appropriate reagents or product in the following examples.

A: Given ; reactant

Q: Give the major product for the reaction. OC(CH3)3 (CH3)2CHCHBrCH3

A: Elimination reaction of alkyl halide: Alkyl halide gives an elimination reaction by reacting with a…

Q: t-Buo Br t-Buo Br Br ECH

A: As you have posted multiple parts of the question and have not specified which part you want us to…

Q: Provide the missing

A: In the given question, a reagent [36] and a transition state [37] needs to be determined.

Q: Provide the missing reactants, reagents, or products for the following reaction sequences

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Q: 1. MCPBA OH PCC Ph 2. 1. CH,MgBr 2. Hо 1. LAH 2. H;O* 1. NaH 2. CH,Br Br

A: Alkene reacts with mCPBA and give epoxide as product. Phenyllithium is a good source of phenyl…

Q: cl 1) H₂, Pdl Ba SD4, Quino line 2) CH3 MgBr, H30*

A: Reagent 1 that is step-1 is Rosenmund reduction to produce benzaldehyde and step-2 reaction involves…

Q: CeHgLi

A: Introduction :  We have to tell the product for this reaction .

Q: НО, H3CH₂CO OH OH

A:

Q: 1) Br2 (H3O) 2) Pyridine (or other base) 3) (CH3CH2)2CULİ 4) H,0 HHOH 10- H HOH Br2 / H2O -OH HHOH…

A: Cyclohexanone reacts with bromine in the presence of base gives 2-bromocyclohexanone.

Q: Y U Li, NH3 1. O3 2. Zn, acetic acid нн W=? PHCH,c-CCH,CH, OHOH V=? H-CEC-H PHCH,C=CCH,CH3 H20,…

A:

Q: но 3 но но Tamoxifen

A: Reagents and reaction conditions for each step

Q: 2. Reaction Fill-ins Predict and draw the product(s) OR starting material(s) for the following…

A: In part a there is ester formation .The reaction takes place between phenol and propanoic anhydride…

Q: t- BUOH i) Mg,dry ether Br OH (3) Hg 0*

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Q: Indicated Reaction by filling in any starting materials,reagents or products as needed

A: Alkene and alkynes give an electrophilic addition reaction with hydrogen halide to form an alkyl…

Q: NaSH Br 1) Hg(OAc)2, CH3CH2OH 2) NABH4 CH;CH,CH,Br

A: According to our policy we can attempt maximum 3 number of subpart. Kindly post rest of question in…

Q: Br (2 Na CH3 DMSO 3 1. ВН. 2. H2O2, NaOH

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Q: CH2 P:lute HBr CH Brz H2O CH „CH, ) BHz THE

A: When a protic acid (HX) is added to an asymmetric alkene, the acidic hydrogen attaches itself to the…

Q: Complete synthesis, show reagents and intermediate compounds.

A: The given amide can be obtained from the acid-amine coupling of diethylamine and…

Q: Provide the major organic product of the following reaction. CH3 HNO3, H₂SO4, A

A: The given reaction is electrophilic aromatic substitution reaction. In this reaction nitration is…

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.