LOH H. available starting materials OH HO + any other reagents + enantiomer target starting materials

Q: 1. Tautomerization of H H;C´ CH3

A: Since you have posted multiple questions, the answer for first question is given below. Kindly…

Q: -OH/H20 ACCI, pyridine H* /H2O

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Q: i. El or E2? | i. Rule? iii. Arrow-pushing Mechanism & Major Product Br NaOEt 'Br KOC(CH3)3

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Q: Fill in the missing reagent(s) that would transform the starting material to the final product. (5…

A: Given:

Q: f) CH3 Raney Ni /H2 g) CH2CN 1. LAH/ ether. - NH-C-CH3 h) 2. H20 ahot meing

A: In the presence of a reducing agent like NaBH3CN the iminium will be reduced to give a new amine.

Q: t-BUOK -> A is the reacich SN1,SN2 ET or E2 and wnat is the Br majar product. er EtONa

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Q: (1) (2) (3) Reagents a Br2 CH212 / Zn(Cu) / ether e i 1. O3 2. Zn / H30* b. CH31 H2 / Lindlar…

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Q: C. CH;OH Is this reaction E1 or E2? elimination product(s) d. NaOH Is this reaction SN1 or SN2?…

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Q: Show the reagents for the conversion below: EtO OEt HO.

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Q: Draw the products of each reaction. KMNO4 Br2 FeBra a. CH3 -C(CH3)3 d. Br2 NH,NH2 b. hv "OH NO2 CH3…

A: Hello. Since the question contains more than three sub-parts, the first three sub-parts shall be…

Q: Show how each alkene can be synthesized by a Wittig reaction

A: Wittig reaction is an organic synthesis reaction which is used to synthesize alkene by reacting a…

Q: 4) Eto ₂ 5) 2-Cyclohexene-1-one O₂Et + ethylace to acetate NaOEt NaOEt ? ?

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Q: Br Pool of choices: OCH₂ ABC CH3OH DEF major substitution product GHI OCH 3 major elimination…

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Q: 8. ******* Which involve large number of organic reaction donot involve and free radicals OA.…

A: Organic reactions are proceeded by many mechanisms like addition, substitution, elimination, etc.…

Q: In an Sn2 reaction with "CN as nucleophile, [CH:CH:CI | CH:CH;OH_ CH;CH;0Tos] reacts faster because…

A: CH3CH2oTosl react faster beacuse it has better leaving group than the other ones. These type of…

Q: stereoisomers. NaOEt 1. Br NaOH Br 2. NaOtBu 3. A Меон 4. Br 2. Which reaction will proceed faster A…

A: 1) Elimination 2) SN2 reaction 3) Elimination  4) SN1 reavtion Reavtion B is faster than A due 1,3…

Q: rxn 1.png R2'NH A + R OR R NR2 (A) (В) A) Addition B Elimination c Substitution D Rearrangement

A: It is nucleophilic acyl substitution reaction which proceeds through addition - elimination…

Q: II. Multistep Synthesis. Supply the missing compounds/reagents. H,C HBr FeBr BH, EtO HC H,C но. Br.

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Q: The correct reagent for the following transformation HO, Jone's reagent H20/H* РСС SOCI2 H2SO4

A: In the given reaction primary alcohol is converted into aldehyde.

Q: a. Rank in order of S2 reactivity (1= most reactive) b. Rank in order of leaving group ability (1=…

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Q: Complete each multi the way. Synthesis A 1) Br2, H20 2) Nao only one stereoisomer required 1) BrMg-…

A: Soln

Q: Circle the least reactive compound in an SN2 reaction. Explain your choice. H H. CH2I CH,CH,I

A: "Since you have asked multiple question, we will solve the first question for you. If youwant any…

Q: a. Rank in order of S,2 reactivity (1= most reactive) b. Rank in order of leaving group ability (1=…

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Q: Identify the missing reagent: 1) ???? 2) NaCN OH CN O PB13 O TSCI (Ts: Tosyl) O CISIME3 (Trimethyl…

A: PBr3 can not be used because it's give SN2 reaction so that configuration inverse and then in second…

Q: e) 9-bromo 5-methyl 2-nonene -----H2, Ni 900°C---------- ? (name, str, stereochem) Cl2, CH2C12 f)…

A: Note: According to our guidelines we are supposed to answer only first three subpart . Kindly repost…

Q: Range order from lowest to highest leaving group TosO- OH-  I-  F-

A: order from lowest to highest leaving group:

Q: Which is the best leaving group for an SN2 reaction? O F- O C- O Br-

A: To identify: The best leaving group for an SN2 reaction.

Q: 1. H3C. CH3 ? ? + 1,2-Product 1,4-Product HBr (1 eq) 2. + Br2 ? ? (1 eq) 12-Product 1,4-Product 3. ?…

A: All these are examples of conjugated dienes which are more stable than simple or isolated dienes…

Q: Q2: OH OH Br Prepare CH;CH2CH-ĆHCH3 starting from CH;CH,CH-CH2CH3 And any other needed reagents.

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Q: а) b) c) OEt

A: When aldehyde or ketone react with diol or alcohol it form acetal.

Q: .2 Circle the best choice for each statement. La to Best Substrate for SN1 Best nucleophile in DMSO…

A: There are some molecules . We have to tell and give explanation the best solvent for SN1 and SN2…

Q: aw the major products for top 2, then indicate products of bottom reagents with reaction with…

A: The major products for the given reactions are attached below.

Q: butan-2-ol → butan-2-one, CH3COCH2CH3. NaOCI НОАС EtMgBr H,CrO4 ether or PCC excess NaOCI ТЕМРО…

A: The oxidation of alcohol can be done via oxidizing agents like chromic acid (H2CrO4). Sodium…

Q: Cl2, Hz0 .CI OH major product

A: Reaction of an alkene with halogen and water converts the double bond to a single bond and one…

Q: PLEASE DRAW OUT PRODUCT H2 Uz, 1 1. HONO 2. 2.CUBr Raney Ni NO2

A: 1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C8H8.…

Q: Carboxylic Acid Resolve the reactions.

A: KMnO4 converst alkene to cis-diol K2CrO4 oxidizes R group with at least 1 benzylic CH to COOH Jones…

Q: Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2

A: Introduction: NaNH2 is a strong base. It is often used for deprotonation in weak acids or also for…

Q: A. Rank the following alkenes in the order of increasing stability (1 = least stable, 5= most…

A: 8. SN^2 reaction is susceptible towards steric repulsion. Hence, lesser is the steric repulsion…

Q: What is the main product of the following reaction? Show every step of the mechanism please

A: This is an example of Haloform Reaction.

Q: Draw the alkynes formed when each dihalide is treated with excess base.

A: a) When the given compound (1,2-dichlorobutyl)cyclohexane is treated with an excess base such as…

Q: b) CH3-CH-CH-CH; ОН ОН frpm CH3-CHOH-CH,-CH3

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Q: Are the following nucleophiles, electrophiles, they be both a nucleophile or electrophile, or…

A: Nucleophiles are those species which are electron rich and hence can donate electron pairs to the…

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: CH3 o-nitrotoluene CH3 NH, CI 2 o-toluidine NO2 NH,HCO2 10% Pd/C Step 1 1) NaOAc, H₂O 2) CI Step 2…

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Q: Draw the enol or keto tautomer(s) of each compound.

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: pla Delow. Reage De us Map d0 than once or not at all. Draw the intermediate products B and C (both…

A: The first step is to start with acetylene as compound A, which react with strong base NaNH2. The…

Q: CH3O HS CH3COO- H20 CH3OH Br Excellent nucleophile Good nucleophile Poor nucleophile

A: Nucleophile : A molecule or substance that has a tendency to donate electrons or react at…

Q: Br NaOH heat Draw E1 Major Product + Draw Minor E1 Product

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Q: What reaction is occurring? Circle one. 1. LIAIH4. -ОН Nucleophilic Substitution Reduction 2. H20…

A: Since LiAlH4 is an strong reducing agent as it produces H- ions in the solution. Hence it reduces…