H. NABH4 `OH 95% EtOΗ ÓCH3 (reduction) ÓCH3 Vanillin Acetate 4-acetoxy-3-methoxybenzaldehyde 4-acetoxy-3-methoxybenzyl alcohol

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

A:

Q: Benzophenone Но. ether -Br Mg° -MgBr + ether Phenylmagnesium bromide Bromobenzene Triphenylmethanol

A: The following is the reaction between Grignard reagent and benzophenone to give Triphenylmethanol

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 mechanism for the reaction?

A: The reaction will have the below mechanism for step 1

Q: Draw the reaction mechanism showing bonds that are broken/formed

A: The reaction is hydrolysis of amide and the mechanism

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: Br CH;OK a) b) Sn1 Sn2 c) d) E1 E2

A: Generally, alkyl halide or alcohols undergo elimination reaction which give rise to alkene.…

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

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

Q: CF3 NH₂ N ม. ผ Br

A: The given reaction is simple nucleophilic substitution reaction.

Q: What is the mechanism of the first step?

A: α-caryophyllene commonly known as α-humulene is monocyclic sesquiterpene which is obtained…

Q: Show the product of the Claisen condensation of ethyl butanoate in the presence of sodium ethoxide…

A:

Q: Draw the product of this nydrogenation reaction. Use wedge and dash bonds to indicate…

A: Interpretation: We have to determine the product for the following given reaction.

Q: Can you answer this question? Identifying the reaction mechanism

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: Br ОН - Br + HO-

A:

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

A:

Q: 2. Selectivity. Show the reaction intermediates obtained after each step and the major product…

A: The details explanation of the organic reaction is given below

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: OTBS I !!! OH Me™! Im Me H OMe OMe OTIPS Br OTIPS tBuLi, Et₂O, -78 °C 83% OTBS I Me Me I !!!! "H OMe…

A: Carbonyl C atom is electron-deficient C atom. Hence, it is electrophilic in nature. An electrophile…

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: What major product (from Figure #4) results from the following two- step reaction sequence (from…

A: Given incomplete reaction is :  What is the major product of this reaction = ?

Q: What is the mechanism of the second step?

A: [2+2] Cycloaddition reaction:- This is said to be this because it involves 2 electrons from one…

Q: N Lo Ph RuCl₂ (PPh 3), K₂ (03 CH3OH, 40 bar H₂ N- Ph

A: In the first step, the three-membered ring with a nitrogen atom (aziridine) reacts with a silane…

Q: H3C° CH2

A: Given reaction is an example of aldol condensation reaction.  Reactants used here : acetone and…

Q: HO z HOH H 요 H₂504 C HO- 0 F 10

A: I think your final product structure is wrong, but your answer (mechanism) is given below

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

A:

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

A:

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.