A) SN1 Br B) SN2 C) E1 CI NaOCH3 heat D) E2 E) no reaction

Q: when necessary. a) b) Br2. H20 HCI d) H2 Ni MCPBA 1) ВН; THF 2) H2O2 NaOH f) H2SO4, HgSO4 H3O*

A:

Q: 0 O O NaOCH3

A: Kindly get the answer given below.

Q: Reagents Available a. CH2=CHCH,CI, AICI3 b. CН-Br2, ОН c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI,…

A:

Q: ОН ОН CHCI3/KOH H+ H. A. dichlorocarbanion B. dichlorocarbene C. trichlorocarbanion D. chlorohydrin

A: The given reaction is a name reaction called Reimer Tiemann reaction.

Q: Select to Draw mCPBA me a 00 1.0₂ 2.Zn/H₂O* Select to Draw

A: 1. Methylcyclohexene reacts with mCPBA produces epoxide. 2. Methylcyclohexene reacts with warm alc…

Q: a) KBr CH3CH,CH,I SN1 SN2 no reaction likely b) CH;CH,OH + H,O SN2 no reaction likely c) CH-CH,ОН…

A: The SN1 reaction is a substitution nucleophilic unimolecular reaction. It is a two-step reaction. In…

Q: (C,H3),P-CH CH3 AICI3 ? H3C (а) (b) H-Br ? ? ? 1. NaNH, NaOH (е) (d) (с) heat Br 2.

A: The first step is Friedel Crafts acylation, second step involves Wittig reaction, since the reagent…

Q: CI. „CH2CI NaOH H2O SN2 E2 mixture of SN1 and E1 CH3 CH;OH `CH3 >

A:

Q: (a) Rank A, B, and C in order of increasing SN2 reactivity. (b) Rank A, B, and C in order of…

A: SN1(nucleophilic substitution unimolecular reaction):  It is two step mechanism reaction…

Q: Calculate the heat of reaction deltaH for the following reaction: 2HCl(g)+Br2(g)——>2HBr(g)+Cl2(g)…

A: We have to calculate ., heat of reaction ∆H for the following reaction: 2HCl(g)+Br2…

Q: a) b) CH3-CH₂- c) d) e) f) 0 O-CH₂-CH2-CH3 de CH3-CH-CH-CH3 CH3 OH -od x OH

A: The given problem is based o nomenclature of organic compounds.

Q: Which group has the highest priority according to the Cahn, Ingold, Prelog rules?

A: five types group is given that a highest priority of according to Change, Ingold, prelog [CIP]…

Q: 1. Name these compounds: a) CH3CH2 а сн он H Br CH3CH₂ CH₂EOK Br b) c) d) CH₂EX Br CH₂C Br CH3CH₂…

A: The organic compounds given are

Q: He SO4 H3C. H HọC CH; CHz GH CHo > = C メ + C=C +H20 CH3 trals-2-buten cis-2-buter 23%

A: Saytzeff’s Rule stated that stable alkene is formed when the removal of hydrogen from β-carbon has a…

Q: Complete the reaction map by matching the answers from A-E. SO3 Brz D HNO3 3, E C FeBrz CH3 CH2 CI…

A:

Q: (c) NO2 NH2 (CH3CO)20 pyridine HNO3 H2SO4 & heat NH2 O2N Br NH2 (d) NO2 3 H2 Ni catalyst А Br Br (e)

A: Stepwise synthesis is given below

Q: Your answer C6HSCH2OCO(CH2)¬CH3 Your answer

A:

Q: 17 ČH2CECH A CHz CEC CHz

A: Reagents are the chemicals that we add to bring about a specific change to an organic molecule. Any…

Q: (a) Rank A, B, and C in order of increasing SN2 reactivity. (b) Rank A, B, and C in order of…

A: SN1 (nucleophilic substitution unimolecular reaction):  It is two step mechanism reaction…

Q: (a-b) (c-d) (e-f) OH CI CI HORE ? NH pyridine -OH HAM S CI LIAIH[OC(CH3)3]3 1. LIAIH4 2. H₂O+ 1.…

A: Lithiumaluminiumhydride is a reducing agent. It release hydride ion (H-). According to Q&A…

Q: one Group 2 two Compound A Compound B Compound C three H CH,CH, H CH,CH, H,CH,C Br Brm F I H,CH,C…

A: Enantiomers : are the non-superimposable mirror images. If the total inversion of all the chiral…

Q: 5. Explain why A is much more stable than B? B NH

A: To explain why compound (A) is more stable than the compound (B)

Q: a) b) c) d) OH | CH3CH₂C=0 CH3CH₂CH₂OH Н OH CHOLL CH3CH₂C=0 Cr₂O72- H₂SO4 CH3CH₂C=0 O O || ||…

A:

Q: CHA ÖH Pocls, 4 CHe CHs 'N- CHg QCH] CHs - HOl eblora eaffeime eaffeine

A: In most keto-enol tautomerisms, the equilibrium lies by far toward the keto form, indicating that…

Q: 4.9 4.15 4.10 1. NaH 2. CH3Br KMNO4, HO- Heat, H20 H2SO4 SOCI2 pyridine POCI3 но 4.14 4.11 pyridine…

A:

Q: `NH H*

A:

Q: (a) HN Brg

A: This is bromination on heterocyclic compound. The position of bromination will be depended on…

Q: Probiem 6.4 Use curved arrows to show the movement of electrons in each equation :Br: b. :O: ö:

A:

Q: N. O2-azabicyclo[2.2.2]oct-2-ene 1-azabicyclo[2.2.2]oct-2-ene O 1-azabicyclo[2.4,2]oct-2-ene

A: The given compound is a bicyclic compound. The root name of the bicyclic compound is given on the…

Q: (a) Br2 FeBr3 (b) NaCN CI (c) HO H,SO, 180 °C Major product

A: “Since you have posted a question with multiple sub-parts, we will solve first three sub- parts for…

Q: Label each C–C double bond as E or Z.

A: The E isomer has the two higher priority groups on the opposite sides. The Z isomer has the two…

Q: PCC (CH,),CHCH, CH,OH Select one: a. CH, CH,CH,CH,COH b. CH, CH,CHCH,CH с. по геаction O d.…

A: PCC reagent is mild oxidising agent. It converts alcohol into aldehyde.

Q: Compound E PBr3 Compound A H₂SO4 Heat Compound B (Major) KMnO₂/ H* Heat i 2-butanone OH + HCN…

A: All the reactions have been completed in the following step.

Q: (a) Rank A, B, and C in order of increasing SN2 reactivity. (b) Rank A, B, and C in order of…

A: Bimolecular nuclephilic substitution reactions (SN2) in alkyl halides follow the order as shown…

Q: OH H2SO4 D. E1 E2 heat OH 1.TSCI, pyridine E. E1 E2 2. NaH

A: Elimination occurs when Alcohols treated with concentrated  sulfuric Acid.

Q: KHS2O3 + H2O --> (?)

A:

Q: A) MoH Hz SOy> acetic acid alconol B) H3C ÒH Hz SO4> dcetic acid alconol

A:

Q: OCH2CH2CH3 a) CH;CH(OH)CHCH(OH)CH(CH:)CH3 H;C. но Br b) e) (CH3):CHCH2OCH;CH3 но. -CH3 CH3 c) bllege…

A: 1. We have to give the IUPAC names of the following given compounds as follows in step 2:

Q: H. Br C6 CI H E2 C2 H. CI Br 1) which one is product? 2) which one is least likely? 2.

A: Introduction: Elimination reaction: Elimination reaction is a reaction in which substituent gets…

Q: A) CH;CH2OH + NaNH2 CH;CH2ONA + NH3. B) CH3CO2H NaOH CH;CO,Na + H2O + с) нC-CH + H2O NaOH HC=CNa +…

A: Given reactions are : For which of the following does the equilibrium favor reactants = ?

Q: H2SO4 CH;CHCH2OH CH3 H2SO4 2 CH,CHCHCH,CH3 CH3 Majo CHaCH-CHCH3 +2KOH Br Br

A: ->H2SO4 is a dehydrating agent which form alkene. ->Alco KOH is used for elimination reaction.…

Q: (a-c) (d-e) (f-g) OH ?? H₂O, H+ CI H₂O HBr OH ?? HIO4 ...H OH H H₂CRO4 O- +Na CH3Br

A: As per the bartleby guidline for answering the multiparts question, I can solve only first three…

Q: Draw the organic products formed in each reaction.

A: Carboxylic acid reacts with alcohol in the presence of acid to produce ester. Boc anhydride reacts…

Q: colaph H B. CH₂CHCH A. Consider the organic structures shown below. Which one corresponds to an…

A: The above organic transformation can be carried out as follows

Q: c) d) e) f) H.C -CH3 -CH3 NaCN ОН 1) BrMg CH OH H₂SO4 CH3 2) HạO* H OCH OCH _NH2OCH3 CH3 CN CH 3 -он…

A:

Q: (e) 1 2 (f) (g) (h) Br (e) H predict the starting compound Cl₂ heat CH3CH₂O + Na K+1 (f) CH₂OH CH3 H…

A:

Q: Rank the following groups in order of decreasing priority. a.−COOH, −H, −NH2, −OH b.−H, −CH3, −Cl,…

A: The following groups are to be ranked in order of decreasing priority: – COOH, – H, – NH2, – OH –…

Q: 1. NaOEt Rxn I 2. Нао CH3OH cat. H* Rxn II

A:

Q: 4. Why do we have to keep Fehling's A separate with Fehling's B?

A: The question is based on the concept of qualitative analysis. We have to explain the reason for…

Q: (i) CH3 CH2CI (h) (е) (g) BrCH2 CH2Br CH3 CH2COOH HOCH2 CH2OH CH3 CH2MG Br

A: