HN CH3B H,0 H* (cat)

Q: 1. CH₂CO3H 2.NaOCH3, CH3OH

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

Q: Draw the detailed mechanism ( please don't use hand raiting please)

A: Grignard reagent involves C-Mg bonding. Grignard reagent is the source of a nucleophile that…

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: Question 5: Determine for the reaction scheme shown. the major organic product 1.2 Li, Et ₂0 CECH a…

A:

Q: Provide a complete mechanism (including all arrows, lone pairs and formal charges) for the formation…

A: This is an example of Claisen condensation reaction

Q: 2 X Ph OH Ph -Ph

A: Through mechanisms of organic reactions, we can find out the type of reactions which are carried out…

Q: Identify compounds A–C in the attached reaction scheme.

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Q: 1) H,Cro, 2) PČI, 3) (CH,CH,),NH (excess) OH Answer:

A: HCrO4 is an oxidising agent it oxidises alcohol in to corresponding carboxylic acid.

Q: Draw the product of the following reaction, indicating the correct stereochemistry. Ili CH,OH H,SO,…

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Q: Synthetic

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Q: can be 4. (a) The following compound synthesised via Robinson annulation. Provide retrosynthetic…

A: Robinson annulation is a reaction which uses a ketone and a methyl vinyl ketone (α,β-unsaturated…

Q: Give reaction of glycol and  ketone with mechanism. Detail explanation

A: Glycol is used as protecting  Group  for ketone and aldehyde

Q: T6DPSO OTIPS Zncl2 Tich TIPSO -> MOTEDPS CHzel, TIPso SPy TMS

A: The first step involved the coordination of the aldehyde with lewis acid ZnCl2, which makes it…

Q: 40 TMSCI, SMTO BV Mg exvev SMTO- MSBV 。 ㅅ got SMTO o OH 7 F- 10 OH

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Q: 6. Br2, aq. NaOH `NH2 1) LDA 7.

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Q: OH HO CH3

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: `NH2 HO. from b.

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Q: Draw the products in the following reaction. Part 1: Part 2 out of 3 of Identify which mechanism(s)…

A: The given reaction scheme is shown below We have to identify the type of reactions. Also, we have…

Q: 7. Provide the major organic product of the following reaction.

A: The reaction of potassium permanganate (KMnO4) with a secondary alcohol would result in an oxidation…

Q: give the full synthesis steps with reagent and condition

A: Robinson annulation consist two reactions. One is Michael Addition reaction and another is Aldol…

Q: A o swobori babisi Onders 20

A: In given reactions, cyclohexanone used to convert required products.

Q: Determine the structures of compounds A and B in the following reaction scheme.

A: 3-bromopropyl benzene reacts with strong base of potassium tertiary butoxide to give allyl benzene.…

Q: Please show arrows for mech. thank you f. он Cu(CH;CN);OTf, TEMPO, air, NMI, bpy Ph OH Ph он РОС,…

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Q: enamine behaves as a nucleophile in much the same way that an enolate anion does, with nucleoph…

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Q: H3C N CH₂CH3 H H2O, H+ ноян

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Q: 14. What is the major organic product obtained from the following reaction? HO. H. PCC CH,Cl2 HO.…

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Q: Provide mechanism

A: The required answer is given below Explanation:Step 1: Step 2: Step 3: Step 4:

Q: NH₂ OH 4-aminophenol + CHO Acetic Acid PC12CHO EtOH OC12H25 4-(dodecyloxy)benzaldehyde C12H25O HC OH…

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Q: H2N CH,COCH,Br S-ル

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Q: cocft HA COLE الموضوع : 2

A: Detail mechanistic pathway is given below

Q: do both or else skip give detail explanation and mechanism...give Typed and mechanism using chem…

A: Alkenes shows the electrophilic addition because of presence of reactive pi-bond. The addition of…

Q: Synthesize the folowng compnd stavting fom bezere (3 (A) (B) CHs Hz N

A: Organic reaction mechanisms:

Q: -Br но-

A:

Q: Can you show me how the mechanism is done? 1.3 BH₂ THF 2. 3 H₂O₂, 3 NaOH, 3 H₂O

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

Q: ca) CI (CH2=CH)2CuLi ether, -78° C (9) 1. 2 CH3CH2CH2MgBr, ether CI 2. H;0* (C) who 1. 2 H3C- -MgBr…

A: In acyl substitution reaction, nucleophile can always attack on electrophilic carbonyl centre and…

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.