MeO CH;CH,NH2 CH,OH + O=

Q: a) b) HO, HO c) OH Br

A: The cyclohexanecarbaldehyde will firstly reduce to alcohol via a reducing agent. The reducing agent…

Q: Protectim of C=0 TSOH benzene HO reglux TS OH =

A: In presence of acid diol can protect carbonyl group.

Q: Write a detailed mechanism. OH りNaoH 2)Brz in CH2C 2

A: First step of the the reaction is Favorskii rearrangement. This reaction is followed as follows:

Q: Q2: Suggest mechanisms for the reactions OH TSOH OH OH TSOH

A:

Q: Complete the reaction and provide a mechanism for the formation of the product Na OCH2CH3…

A: Organic reaction mechanisms:

Q: ОН + H2O

A:

Q: cess CHCH-C 1 KMKO, NaOH HO AICI, H$O. 2. H0

A:

Q: 3. Provide the mechanism for the following rxn: ethanol heat Br a. CH3 CH3 NAOCH3, CH3OH Br b. DH H.…

A: Mechanism of Elimination reaction:

Q: OH Аcetone HO Но HCI HO- OH HO,

A: This reaction is protection of glucose with acetone.     Mechanism:   Step 1: In aqueous…

Q: What is the mechanism for the following reaction?

A: Given reaction,

Q: Provide the mechanism for the 4th and final reaction in this synthesis: KMNO4/H+ НО OH

A:

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

A: Given,

Q: The following electrophilic addition reaction occurs at room temperature. Propose a complete…

A:

Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: ÇOOH CH,OH CH,OH (1) LIAIH, (i) H̟O HNO, / H,SO, `NO,

A: The formation of alcohol from a carboxylic acid is a reduction reaction. It takes place in the…

Q: Provide the mechanism for the 2nd reaction in this synthesis: H2O CI

A: Step 1: Acid chloride reaction with Grignard will give the ketone. Step 2: keto compound react with…

Q: Show the complete mechanism for the reaction of t-butyl bromide with water to produce…

A: Given :-  t-butyl bromide + water →  2-methyl-2-propanol  To draw :-  Complete mechanism of reaction

Q: Write a detailed mechanism for this transformation. OH HCI НО НО H2O -OH

A:

Q: Propose a reasonable mechanism. H*/ H2O

A: Given reaction,

Q: Write the complete mechanism for the hydroxide ion catalyze reaction of cyclohexanone and…

A: Hydroxide ion (OH-) act as a catalyst which can abstract the acidic alpha proton to form the enolate…

Q: Br Br2 Br hv HBr NBS Br HBr Br hv HOOH

A:

Q: Provide the mechanism for the 5th and final reaction in this synthesis: OH KMAO4

A: This is an oxidation reaction.  Here secondary alcohol is converyed into ketone using potassium…

Q: CrO3, H2SO4 acetone

A: CrO3.H2SO4 also known as Jones reagent which is used for oxidation .It oxidizes primary alcohols to…

Q: 0. 1) СО2, Р, д 2) Н2О, H*

A: This is a klobe synthesis  in which major product is salicylic  acid

Q: 4. Provide the reagent(s) needed to complete the following reaction scheme. Provide the complete…

A:

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

A:

Q: Explain and detail the reaction mechanism: NaBr + H2O + n-butyl alcohol = ?

A: In this que, acidic condition is missing, this reaction cannot take place in absence of acidic…

Q: ~NBU2 HO NaOH H. CI ELOH

A: The first step of the reaction involves the acid-base reaction. The NaOH being a strong base will…

Q: Draw the product of the given reaction sequence. Select NaOCH3, CH;OH

A: Robinson annulation combines a ketone and an (alpha, beta) unsaturated ketone. The reactions are…

Q: Show a detailed mechanism for the following reaction. 1. Cl2, NaOH 2. Hзо*

A: Applying concept of haloform reaction followed by acidic hydrolysis.

Q: Provide the mechanism for the following transformation: NaCN CN + Naci

A:

Q: TSOH MeOH

A: Product for the given reaction is,

Q: 20) Provide the mechanism and draw the structure of the major product of the following reaction:…

A:

Q: Give a complete mechanism for the following Reaction: CI NH2 NH2 NANH2 / NH3 ČH3 ČH3 CH3

A:

Q: i. H,C CH3 CH, c-CH CH CH CH H,C CH3 Он Br ii. HO HBr

A: Organic synthesis examples.

Q: Provide the mechanism and the product for the following reaction: Br* MeOH

A: A species having a positive charge is known as the electrophile whereas the species having electron…

Q: CH3 NHCH3 CH3 CI CH,NH2 triethylamine

A:

Q: Br2 NEIS A CH,Cl2 CH,BrO;

A: Reaction 1 : Bromine addition to olefin. Reaction 2 : E2 elimination.

Q: Provide the mechanism for the following reaction. O H H Me 2 Li, NH, then Quench H H Me

A: The given reaction is,

Q: но. CH3 NaOH aq.

A:

Q: а. b. HO,

A:

Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

Q: Meo ACOH MeO. NH2 NH

A: This is two step process. First step is the acid catalyzed imination of amine with aldehyde. second…

Q: CH2Br 1. NaNH2 → A CH3CH2C=CH В

A: We have to draw the products and give the mechanism for the formation of A and B as follows in step…

Q: Br Mg ? →? H

A: The given reactant is Bromo benzene.

Q: Provide a detailed mechanism for the following reactions and determine the major product: HO. se +…

A: Note - The given question is a multipart question, hence I solved first three questions according to…

Q: Provide the mechanism for the 2nd reaction in this synthesis: D2S04 PSO4

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.