HBr ? peroxides

Q: from OH

A:

Q: As shown below, pyridine -oxide G can undergo electrophilic aromatic substitution with electrophile…

A:

Q: (b)

A: We have to carry out the given reaction conversion.

Q: 3. Propose a plausible mechanism for the following transformation НО. YOH H2SO4

A: Applying concept of formation of electrophile and electrophilic substitution on benzene ring.

Q: Propose a detailed mechanism for the following reaction: HO OH H₂SO4 O y

A:

Q: How will you Synthesize benzyl the following morecule from bromide ?

A: In this question we will synthesized the given compound by using benzyl bromide  You can see details…

Q: 14. Propose a mechanism for following transformation. M₂O 0

A: In this question, we will write the details mechanism steps by using curved arrows for the given…

Q: 2. Propose the synthesis of following compound:

A: In this question, we will write the synthesis of the given compound.  We will used benzene ( as a…

Q: NBS hv

A: Here we are required to predict the product of the reaction.

Q: Propose a mechanism for the following reaction:

A: The given reaction is represented as follows:

Q: Propose a reasonable mechanism to explain the following Reactions.

A: Mechanism of above reaction is given below.

Q: Give the structures of compounds A through F in the following series of reactions. HNO3 H;కం CI A B…

A:

Q: 5. Propose a plausible mechanism for the following transformation:

A: Given that : We have to propose a mechanism for the following transformation :

Q: Propose a synthesis of the following compound starting with benzene and other compounds of four…

A: The reaction of the acid chloride with the aromatic compound to yield the acylated compound is…

Q: Propose a synthesis for the following compound from benzene. Br

A: Given compound: We have to synthesize the above compound from benzene.

Q: The following compound undergoes Benzilic Acid Rearrangementto yield ahydroxyacid salt. Proposea…

A: In benzylic acid rearrangement, OH- (nucleophile), attacks the partial positively charged C of…

Q: ive the structures of compounds A through

A: In the given mechanism reactant is Benzene. Due to friedel  crafts acylation the product A will…

Q: Propose a synthesis of the following molecule starting from benzene. O2N CI

A:

Q: Propose a detailed, step-wise mechanism for the following transformation, make sure to SHOW all…

A: Desulfonation reaction In organic chemistry, the desulfonation reaction is the hydrolysis of…

Q: Propose a predict the major product in each of the following reactions

A:

Q: Ph * Ph Bv 014 Br CN Ph. with

A: Applying concept of organic synthesis and reaction mechanism.

Q: How would you accomplish the following synthesis?

A:

Q: 2b. Device a synthesis route for the following: Hg(OAc): NaBH, он p-TSCI pyridine a) b) KCN d)

A: Oxymercuration reaction: The alkene gives an electrophilic addition reaction to form alcohol. When…

Q: Provide all reagents to accomplish the following synthesis:

A: NBS is N-bromosuccinimide is used for allylic substitution. Thus Br group is substituted at the…

Q: The least reactive molecule towards nitration reaction is Select one: O Ethylbenzene O benzene o…

A: in the nitration, the rate/reactivity is enhanced by the electron-donating substituents attached to…

Q: Suggest efficient synthesis for the following transformations. `Br (a) он (b) ICH3

A:

Q: What would be the product of the following reaction? Suggest a mechanism. H+

A: The reaction of a reactant thio-ester undergo acid hydrolysis is as follows, firstly lone pair of…

Q: a) HBr

A:

Q: OEt 1. NaOEt 2. H3O*

A: The given reaction is,

Q: 2. Propose a reasonable synthesis of compound 2 from compound 1. Use no more than 4 steps. Он он он…

A: "Ardnt-Eistert Homologation" is mainly used for the conversion of a carboxylic acid to larger…

Q: Propose a synthetic method for the following compound:

A: The given compound can be prepared by using benzene which shows electrophilic substitution of…

Q: Present a plausible synthesis of the following transformation below. Explain

A:

Q: iv) NGÔM, HO Heat

A: Note : Retro aldol followed by intramolecular aldol condensation. (For mechanism, see below).

Q: А B C D Br Br

A: We have to rank the order of the reactivity for the given compound

Q: Give the major product of the following reaction

A: Given reaction,

Q: 5. Outline a stepwise mechanism to account for the following reaction. [Hints: The mechanism begins…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: 1. Propose two syntheses of the following compound, each using a different Gilman reagent.

A: Gilman Reagent is the Lithium dialkylcuprate. It is used for the formation of C-C bond.

Q: How would you carry out the following synthesis?

A: a. Friedel-Craft acylation followed by bromination then Grignard reagent preparation and then…

Q: B) The following sequence of reactions was employed during synthetic studies on reidispongiolide A,…

A: All details explanation in Handwritten solution.  Step first ring opening  of epoxide  then…

Q: I

A: We have to synthesize the given compound.

Q: 3. Propose your own synthesis of compound C. HHOH readily available precursors C

A: This is a multi-step synthesis. The final product (c) can be obtained from the readily available…

Q: HBr peroxides

A:

Q: II. Propose a suitable synthetic route to carry out the following transformations.

A:

Q: Propose a mechanism for the following reaction. КОН in MeOН

A:

Q: HBr HBr a) b) ? peroxides

A: Alkenes reacts with HBr without peroxide and undergoes addition reaction via carbocation formation…

Q: Propose a mechanism for the following reaction:

A:

Q: (a) CHS 1 OC-Mn ос ICO -CH₂-> +PPhy>? do

A: The transition metal complexes are those in which the central atom bonded to the ligands is a…

Q: HC HC

A:

Q: Propose a synthesis of the following product beginning from benzene. HN.

A:

Q: сно

A:

Q: Proposing a plausible arrow pushing mechanism for the following transformation. Show all steps. H3O*…

A: In the above reaction, the double bonded O of the ester group will take proton first. Now the other…

Q: 17. Provide a curved arrow mechanism for the following transformation. Br NaN, DMSO

A: As shown in the reaction, the rection follows SN2 pathway because the product is inversion in…

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.