13) Propose a synthesis: moold, H3CO rOCH3

Q: но но, HO,

A: Conversion of one compound to another takes place with the help of various reagents.

Q: O Provide the major product of the following reaction. AICI3

A:

Q: Propose a plausible mechanism for the following transformation. OH [H,SO] MESH Mes

A: Sequence in the mechanism :-  Protonation of etheral oxygen Attack of nucleophile to the most…

Q: IV. Propose a plausible synthesis for each of the following transtormations: 1. 2. Br Br CI ОН 3. H…

A:

Q: Waite the mechanism of Action below ReactHon and IR Spectra of product NBS (Phloz}, tolvene Toluene

A:

Q: Q3. Let's try to suggest a synthesis for para-nitrotoluene from benzene, as shown below. CH3 ? NO2

A:

Q: 10. Provide a synthesis for the following molecule. S

A: The steps involved in the above reaction are abstraction of proton from alkyne, nucleophilic attack…

Q: from OH

A:

Q: (i) How would you synthesis the following using the Mitsunobu reaction. Show the mechanism. , H O…

A:

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: Starting from Cyclohexanone, propose a synthesis of: 'N

A: ->First of all cyclohexenone reacts with dimethyl amine in acidic medium. ->Then we use…

Q: COOH

A: Targeting compound can be synthesized in different ways. But, we will discuss with the most…

Q: B3. Write a detailed mechanism for the following Knorr Synthesis 1) (BUO-NO (0.5 equiv) , HCI A…

A: Preparation of pyrrole compound by using beta amino keto-ester and beta-keto ester is called Knorr…

Q: 3. Provide a synthesis of the following molecule starting from benzene. Br NO2

A: - In order to get the desire product one should follow the following steps :-  Step 1 :-  FC…

Q: 2. Propose a synthesis for the following compound starting with benzene. NO, CI

A:

Q: ОСНЗ ОСHЗ Он OCH3

A: The chemical reaction via which one organic compound converts into other is known as organic…

Q: Suggest likely a mechanism for the following reaction: PPO OPP- CH3

A:

Q: 2. propose a Synthotic soute Cinclude rectancts/cegeants/solvents etc.) to Your molecule from…

A: Given compound is propanoyl chloride.  Let's see synthesis of this molecule from ethylene.

Q: Boc- `N H CO₂Me i) 9-BBN ii) Ph-Br, 5 mol% PdCl₂(dppf), K3PO4, DMF Вос. `N H CO₂Me

A:

Q: Perform retrosynthetic analysis for the following target molecules and show how TO torward synthesis…

A: It is a technique used for solving complex molecules. The target molecule is transformed into…

Q: H,SO4 + CH3-0-H OCH3

A: The given reaction is the addition of hydro-alkoxy in an acidic medium. The first step is the attack…

Q: Q3/ Suggesting mechanism for the following reactions: OH OH сно СHCI, NaOH 70° 1 Add File сн, он CH,…

A: 1) First reaction is known as Reimer Tiemann  reaction . 2) The reaction of Alcohol with H2SO4…

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

A:

Q: %3D HO

A:

Q: Propose a mechanism for attached reaction:

A:

Q: 3. Propose a reasonable synthesis for the following transformation. H

A:

Q: Propose a synthesis for the following: Br NO2 CI NO2 он CN

A: The synthesis can be done as:

Q: 0. 1) СО2, Р, д 2) Н2О, H*

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

Q: 1. (CH3CH2),CuLi 2. H20, H*

A: [As per rules only first question could be answered]   Organocuprate, a soft nucleophile, preferably…

Q: SA. Identify the product and write a detailed mechanism to account for its formation CH3 H,o PRODUCT…

A: Since you have posted multiple questions, we are entitled to answer the first only.

Q: B) Provide the minimum reagents required for the following syntheses below. Me. Me. OMe HO,

A: In the given reaction 1, ester undergoes hydrolysis to produce carboxylic acid in the presence of…

Q: CH3 CH=CH, H*

A: The given reaction, When 2 molecules of styrene is treated with aqueous sulfuric acid,…

Q: Propose a detailed mechanism for the reaction below. لعلام , AICI3

A:

Q: 21) Propose a mechanism for the following reaction. OH H2O, H*

A: Alkenes undergo addition reactions in presence of water and acid. The reaction proceeds via the…

Q: но O:

A: we know that, if attack of halogen on ring is called electrophilic aromatic substitution.

Q: Provide the structures for the synthesis below. Br NaOEt H,O c + D + e B.

A: The reaction schema given is,

Q: N02 Nitration conc. HNO3+ conc H2Sou Bentene NitHobenzene Mechanism:- Nittoanium ion NO2 + 0=N=0 →…

A: First reaction is the nitration of benzene. Nitration of benzene takes place in presence of…

Q: 15. Propose an electron arrow pushing mechanism for the following reaction. H2SO4 SO3H

A:

Q: iv) NGÔM, HO Heat

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

Q: 2) you Isobutane

A:

Q: Br Br2 OH

A: In the given reaction, the first step of the reaction is the addition of the bromine to the double…

Q: Propose a synthesis of the following: A) OH осн, но- B) CH, CH3 H3C OH H3C. CH H3C.

A: We are required to  design  synthesis for a certain chemical reaction using different reagent to…

Q: .Me N. Me. Me. Me Ме Me

A: The reaction taking place is given as,

Q: 5. Provide an efficient synthesis for the following transformation. Synthesis with the fewest steps,…

A: When a molecule has O=C(R1)-C=C-R2 structure, it is termed as the alpha beta-unsaturated carbonyl…

Q: Propose a synthesis of the target molecule from the starting material(s) provided Please be…

A: Step 1 : Hydrogenation. Step 2 : PCC oxidation of secondary alcohol. Step 3 : Acetlide addition to…

Q: Propose a synthesis for the following compound from benzene. OCH3

A:

Q: 3.4 Propose a mechanism for the following reaction: CI NaNH, Liq. NH3 NH₂

A: In the given reaction the chlorobenzene reaction sodium amide to form aniline. The reaction is…

Q: Propose retrosynthesis and later synthesis COOET EtOOC CH3

A: By retrosynthetic analysis, we actually try to move backwards on the synthetic line and try to reach…

Q: ОН HO СООН C-OCH3

A: There is the conversion of o-hydroxybenzoic acid to o-hydroxyacetophenone.

Q: Propose a plausible mechanism for the followng reaction INa, NH3 (liq) 2 NH CI

A: Reduction is the reaction of addition of 2H atom across carbon-carbon double bond or triple bond…