~NBU2 HO NaOH H. CI ELOH

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: Supply the missing compounds in the following synthesis scheme. 1. NaNH2 (3 equiv) H CCI4 Br2 1.…

A:

Q: Draw a reasonable mechanism for the following reaction HO-S=0 HO OH OH

A: In this question, we will draw mechanism for each Reaction.

Q: Startng product wait oan

A: Dehydration of alcohol takes place in presence of dilute sulfuric acid. Initially oxygen of alcohol…

Q: Chemistry complete the synthesis mechanism, show each step H,N

A:

Q: i-step synthetic pathway below by filling in the missing products along Synthesis B Synthesis C…

A:

Q: What would be the major product of the following reaction sequence? H+ ? CH3OH OCH OH OH OH он OCH3…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: Provide the mechanism for the 2nd reaction in this synthesis: D20 o-k

A: This can be explain with the help of chair for. In the product the D group is present on the dash ,…

Q: Provide the mechanism for the 1st reaction in this synthesis: ВНЗ/ТHF

A:

Q: NO2 Br

A: The conversion is given below in pic.

Q: CH2OH но- H- (а)* NaOH H. OH H20 OH CH2OH +

A: Base catalyzed enediol rearrangement of monosacchardies : In the presence of basic solution a…

Q: In this step alkyne amion is alting and it is attacking acting acting as a electrophile Ho as a…

A:

Q: OH ONLY CI

A: See synthesis below.

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: CH,OH OH + CO2 H. OH H ОН OH ČH,OPO,2 ČH,OPO,2

A: First aldehyde to carbo

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: SH 5 steps

A:

Q: OH (TM) (CH₂)4CH3 (SM) H

A: Here we have to synthesize the following given target compound from the given starting material by…

Q: e Tson t

A:

Q: Br. SO3H

A: Ans  Electrophilic substitution reaction initially sulphonation then bromination of benzene

Q: GS Q5 Show all missing reagents and intermediates in the reaction sequence below. Put the…

A:

Q: HO Provide a mechanism for the transformation below. HO H,O/ CH;OH :0:

A: A reaction mechanism is the order of basic steps by which a chemical reaction occurs. A reaction…

Q: Enio bns 200 HO HO ONLY

A:

Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

A:

Q: Propose a mechanism for attached reaction:

A:

Q: Propose an efficient synthesis CI MeO O OMe OEt COOH Br NO₂ O EtO

A: We have to propose an efficient synthesis.

Q: HO 1. LIAIH4 2. H20 HO HO HO.

A: Mechanism

Q: provide a reasonable mechanism for the following reaction CX НО, OH H₂SO4 (cat)

A: Basically this reaction ia used in protection of aldehyde and ketone in order to prevent the…

Q: H2N. Br N° H2N

A:

Q: Question attached

A: In an organic reaction, a nucleophile attacks an electrophile.

Q: 38) Complete the following reactions with the proper major products. SO3/H₂SO4 Br2 FeBr3 MeCOCI…

A: Step 1 : Fridel craft acylation. Step 2 : Ortho isomer ( Sulphonation takes place at para position…

Q: Which reaction steps would you use to carry out the synthesis shown? phmylacetyieme 1. Na/NH3;…

A: here 1-alkyne react with base , base abstract the proton of alkyne and formed negative charge  2-…

Q: ö: Br: H,0 heat ОН DH

A:

Q: H. HEAT ENDO PRODULT Exo FRODUCT XO

A: Both are Dieles Alder reactions and give Dieles Alder Product via [4+2]π cycloaddion reaction.  You…

Q: Propose this mechanism

A: Given reaction,

Q: b. Pt catalyst C2H5-CEC-H + H2

A: Interpretation- To complete the above reaction which is given above in the question -…

Q: Arrow-pushing Instructions MeOH Draw curved arrows to show the movement of electrons in this step of…

A: Given reaction is :  Draw the curved arrows to show the movement of electrons in this step of the…

Q: Br

A: Organic reaction mechanisms.

Q: Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible…

A: The complete reaction is given below.

Q: Draw a mechanism that satisfies the transformation below. OH Cl2 Ph H20 Ph

A: When alkene reacts with Cl2 to form cyclo chloronium ion as an intermediate in this reaction, which…

Q: How do I make a mechanism for this reaction

A: The given reactant is a trans alkene and the reagent is m-CPBA. When the alkene is added to m-CPBA,…

Q: CI Br. NO2

A: Answer:- This question is answered by using the simple concept of chemical reactions of benzene…

Q: OH но OH BF3'Et20 HO HO `OH

A: Alcohol react with lewis acid and carbon attached to -OH becomes more electrophillic which further…

Q: Provide the mechanism for the 1st reaction in this synthesis: OH .CI SOCI2 Mechanism NOT Required

A:

Q: CH,0-P-8 OCH, CH;0O, NaOCH3 H. OCH3 + CH,0 OCH3 CH;OH CH;0 CH;0

A: This is an example of Wittig-Horner reaction

Q: nothe Write a detailed mechanism for this transformation но. HCI HO H20 H

A: The given reaction is an hydrolysis of ether

Q: HBY Cexcess) -> 4.

A:

Q: What is the final product of the multi-step synthesis sequence of reactions shown? NaNH, NH, LINH;…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: OH "R/S Br Design a synthesis for this reaction above:

A: For the given transformation, alcohol is an potential intermediate and it undergo oxidation to…

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.