а. 1) LIAIH4 pyridine Ph3CCPh Ph3CH PHCH2OH + 2) H-О, H*

Q: Suggest the reagents and show mechanism

A: In this question, we will find out the appropriate reagents and also shows the reaction mechanism…

Q: Predict the major product of the following reaction. A B 11 IV OH H₂O H₂SO4 OH ווו E OH IV Give…

A: This is hydration reaction. Alkene react with H+ and H2O to give water. Addition of water take place…

Q: mechanisms for the following reactions. (a) (b) (d) (f) ropose mechanisms for the following…

A:

Q: PROPOSE A SUITABLE SYNTHESIS TO ACCOMPLISH THE FOLLOWING TRANSFORMATION он

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: None

A:

Q: Two mechanisms are among those that have been postulated for decomposition of aryl diazonium salts…

A: The objective of the question is to understand how kinetic studies can be used to determine the…

Q: 11 Chemical Formula: C₂H₂O 12 cat. NaOMe B Chemical Formula: C14H1602 NaOMe MeOH 13 Chemical…

A: Michael additionAldol condensation

Q: Show how (A) can be converted to tolciclate. Use 3-methyl-N-methylaniline

A:

Q: Suggest a synthesis for the following compound from benzene

A: Given is organic molecule.

Q: (a) _MgBr + O=C=O

A: In the first reaction, Phenyl magnesium bromide is reacting with carbon dioxide. In carbon dioxide,…

Q: a) (b) ON c)

A: The given compounds are synthesized from alkyl halide and aldehyde or ketone has to be given.

Q: (c) Propose a plausible mechanism for the following transformation: H [H*] MeOH OMe NH₂

A: Amide are organic compounds, they have O=C-NH functional groups.They are reactive due to the…

Q: 13.43 Predict the products of the following reactions. (a) 。 (b) (c) + OMe CN 우 A

A: Since you have asked question with multiple sub parts. we will solve the first three subparts for…

Q: Predict the product of the following reactions and show the reaction

A: The objective of this question is to propose reaction mechanisms and predict the products of…

Q: (c) With reference to the following reaction scheme: Me Mé N Boc 20 OMe DIBAL, toluene, -78 °C then…

A:

Q: Propose an efficient synthesis (with mechanismsOfor each of the following transformations:

A:

Q: For the following transformation, predict the major product, and suggest a mechanism for its…

A: Gem-dihalides or vicinal dihalides on reaction with excess of sodamide form alkynes.

Q: Predict the MAJOR product by proposing a plausible step by step mechanism. Indicate stereochemistry…

A: Ring opening  of epoxides  in acidic  medium  through  SN1 Type mechanism  attack preferred.

Q: H2SO4 H20

A:

Q: NaOEt

A:

Q: Explain  and  describe details for this mechanism.

A: Acid protonated the carbonyl oxygen and makes it electrophilic or increases ots electrophilicity

Q: 19.73 Propose an efficient synthesis for each of the following transformations: (a) 0-0 (b) (c) Br -

A: Step 1:a) The product is synthesized from the starting material by using the two-step reaction…

Q: Suggest reagents and reaction conditions for each of the following reactions: (a) (b) (c) (d) O H O…

A: The questions discusses about some of the transformations related to the carbonyl functionality…

Q: Predict the products for the following reactions, showing the complete mechanism and appropriate…

A: Given are organic reactions. Given reactions are halogenation reactions of alkene.These are addition…

Q: (1) P (b)Give products and mechanisms for the following reactions. он CH₂SO

A:

Q: (b) Provide the structure of the major products in the reactions below: (i) (ii) НО НО- НО OH НО НО…

A: Organic transformation

Q: Br H3PO4 EtzN DMSO

A: The reaction of an alkyl halide that involves the formation of alkene as a product when it is…

Q: As shown below, the drug novocaine can be prepared according to the retrosynthetic sequence…

A: Since you have asked a question with multiple subparts, we will answer only first 3 subparts for…