What major product (from Figure #4) results from the following two- step reaction sequence (from Reaction Sequence # 4)? Reaction Sequence #4 МСРВА H* MAJOR PRODUCT? MeOH ерохide Figure #4 OH OMe OH Meo OH OH OMe OMe compound A compound B compound C compound D Hint: the reaction of the epoxide with methanol (MeOH) is performed under acidic conditions, so please make sure that you understand which carbon in the protonated 3-membered ring epoxide gets preferentially attacked by the methanol nucleophile. compound A compound B compound C compound D

Q: CH, CH, H,C- -CH H-C O a SN1 O b. E1 Oc SN2 Od. E2

A:

Q: 1. Provide a complete curved arrow mechanism for the most straightforward conversion of 1 to 2. Br…

A: Given conversions are

Q: What is the major product of this reaction? HI (1 mol equivalent) HO, HỌ. OH OH

A:

Q: HO. H2 S04 Hz O Heat

A: Acid catalysed dehydration of Alcohol

Q: A (1E,4E)-1,5-bis(4-methoxyphenyl)penta-1,4-dien-3-one C19H1803 MW:294.35 g/mol equiv. 1.1 NaOCH…

A: In the given reaction formation of an enolate by base abstraction of an alpha proton, followed by…

Q: What is the name of the major product of the following reaction? 1 equiv Br₂ CC14 Br O O…

A:

Q: OH 1. PBr3, pyridine 2. NaCN, DMSO

A:

Q: Br NH2 1. NaNH2, NH3(1) 2. H;O*

A:

Q: What major product (from Figure #1) results from the following reactio (from Reaction #1)? Please be…

A: This is SN2 reaction mechanism. And in this mechanism inversion in the configuration so that's why…

Q: .זכ Hy POy MBS Br N- Dromo Suceinimide

A: N-bromosuccinamide is a chemical reagent which is used in radical substitution, electrophilic…

Q: Can you show the mechanism and explain the steps

A: Dehydration of alcohol in the presence of acid leads to the formation of an alkene.

Q: Confused on how to continue with this mechanism reaction

A:

Q: CH3 CH;=CH(CH2)2 , 'N' 35-47% ČO,H

A: In this question, we will write the mechanism so first we need to redraw the starting material in…

Q: Br Ph Me Sml₂ (2 equiv) THF, -78 °C 95% Ph OH Me

A: The SmI2-mediated reaction is initiated by a single-electron reduction of a halide which generate a…

Q: Draw the mechanism for this reaction. HO H,SO4.

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: f) of 1- 2- H* Br 3- H*, H₂O 1-03, CH₂Cl2, -78 °C 2- CH3SCH3 C8H1402

A: Given,The reaction:

Q: HBr, ROOR

A: Addition of HBr in presence of peroxide follows Anti-Markonikov's addition around alkene in which…

Q: Propionaldehyde undergoes an aldol condensation to form the aldol dehydration product. HCI = Product…

A:

Q: CeHgLi

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

Q: H HNO3 H2Sou 여 N Но

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: ОН б HO НО, "" 'Н НО ОН Но,

A: Benzene with hydroxyl groups in 1, 3, and 5 positions is called phloroglucinol. The phenyl ring with…

Q: CH,MgBr H,O Et,0

A: Reaction of Grignard reagent with ester: The Grignard reagent react with ester produces tertiary…

Q: 1.NaH/MDSO/CH3I 2.HNO3/H,SO4 3.Fe/HCI CH3 H3C 'N' NH 4.1.HCCOH/Heat 2.HNO/H2SO4 'N' N.…

A:

Q: OMe OMe tert-Butanol H2SO4 Acetic acid OMe OMe

A: Below attached file showing the details step wise mechanism to the given reaction.  All the best.

Q: Draw detailed mechanisms for the following transformations Мео. Br2, NaOH Meo, NH2 `NH2 H20

A: The details solution for this reaction is provided below in attach image.

Q: Но Na2Cr2O7 H₂SO4

A: The reagent given is = Na2 Cr2 O7 / H2 SO4 .It is a strong oxidation reaction .sodium…

Q: Br dilute OH

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Can i see the mechanism for this reaction

A: Given,

Q: CH3 CH3 CH3 EH3-C-CH=CH-CH3 + HCl CH3 -C-CH-CH2- CH3 CH3 CI

A: This reaction of Electrophilic Addition reaction, first alkene attack on H+ as a nucleophile. then…

Q: After drawing a mechanism for this reaction determine which intermediate cannot be formed. A H…

A: A question based on reaction intermediate. Five options are given, the most inappropriate…

Q: R-O-O-R

A: This is Free radical decarbonylation. 1st product is without radical rearrangement via less stable…

Q: What major product (from Figure #3) results from the following two- step reaction sequence (from…

A:

Q: H. NABH4 `OH 95% EtOΗ ÓCH3 (reduction) ÓCH3 Vanillin Acetate 4-acetoxy-3-methoxybenzaldehyde…

A: NaBH4 is mild reducing agent it reduces aldehydes and ketones to corresponding alcohols.  NaBH4…

Q: H3C, CH3 H3C N. HN. HO, N. N. ČH3 ČH3

A:

Q: Draw the mechanism for this reaction.

A: The given reaction takes place by Markovnikov's rule. First of all, water gets protonated to form…

Q: 3. For the following reaction draw all the possible products and identify the major product(s) and…

A: We know  H2O is polar  solvent.  The possible intermediate and product of following reaction are as…

Q: CH2 II NH HCI H20 O. H H3C H H3C HO,

A: