NaOH N2OCH3 H3CO OCH heat

Q: Be sure to answer all parts. Predict the product and draw a stepwise mechanism for the following…

A: For the above conversion use unimolecular substitution reaction.

Q: 2. Show how to accomplish the following transformation: OCH3 NHCH3

A: Hydrolysis of amide followed by esterification leads to the desired product.

Q: с o Br Br Br Br o o Br

A: As per Bartley guidelines, and expert is allowed to answer first three subparts of a question.…

Q: Select the major product of the reaction sequence below. CH,CH2CH3 H,C CH2CH3 Br 1. KOH/ 200°C 2.…

A: The details solution for this is provided below in attach image.

Q: с. H2N° HO, SOCI2 (еxcess) N-CH3 CH3

A: Detail mechanistic pathway is given below to find out the final product

Q: OEt EtO OEt

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Q: What would be the major product of the following reaction sequence? H+ ? CH3OH OCH OH OH OH он OCH3…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: Draw a stepwise mechanism for each reaction. Br + CH3CH2NH2 NaOH 'N" + H20 + NaBr a. Br ČH,CH3 NABH4…

A: When aldehyde or ketone reacts with NaBH4, they get reduced to alcohol. Cyclization is defined as…

Q: CH3 Na/CH3ОН NH3 (liquid)

A: Given reaction is example of birch reduction.

Q: Select the structure of the major product in the following reaction. CH;COOOH

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Q: and Н CH3 ОН

A: We have to synthesized the following transformation where you utilise both reagents somewhere in the…

Q: OH HO Br HO

A: The question is based on the concept of chemical conversions. we have been given reactant and…

Q: Draw a stepwise mechanism for the following reaction: HBr HO, Br Part 1: HOBR Br H,0 HO view…

A: Alcohol reacts with a hydrogen halide to form an alkyl halide. The reaction proceeds with an SN1…

Q: Draw a stepwise, detailed mechanism for the following reaction. он CH30. CH;O. H,SO4 + H20

A: The mechanism can be shown as: Step 1: Protonation of the alcohol in the presence of acid.

Q: Show a possible mechanism for the following reaction 1) LAH (xs) 2) H3O* 3 MeOH

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Q: NaOH NaOCH3 Choose. H3CO OCH3 heat

A: The primary carbanion is more reactive then the secondary and tertiary one .

Q: 2. Propose a mechanism for the following transformation. Explain why one OH group leaves…

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Draw the transition state for each attached reaction.

A: Transition state is the state which represents the bond breaking and bond forming state.If the…

Q: Please help! Provide the reagent needed to complete each transformation

A: NOTE: please note according to our policy , we can only answer first three subparts of a question.…

Q: え 一X HO OH HO 人

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Q: Br CH3-CEC -CH3 2HB1 CH3-Č-CH2-CH3 + Br

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Q: G. Н. I.

A: "Since you have posted a question with multiple sub-parts, we will solve the first thee subparts for…

Q: Which reaction A through D yields hexan-1-ol? Click on a letter A through D to answer. но 1. LIAIH4,…

A: Solution :    Organic reduction of carbonyl compounds taken place by a different reducing agent .…

Q: Ffor each reaction below. Br2 a FeBr3 poiw H2SO4 SO3 CI AICI3 OH H2SO4 e HNO3 H2SO4

A: Few questions based on aromatic electrophilic substitution reaction, which are to be accomplished.

Q: Label each step in the following synthesis as either a functional group conversion or a traction…

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Q: Show how to convert the given starting material into the desired product. Note that some syntheses…

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Q: HO Provide a mechanism for the transformation below. HO H,O/ CH;OH :0:

A: A reaction mechanism is the order of basic steps by which a chemical reaction occurs. A reaction…

Q: MeH Ме ОН N. H. Fill in the necessary reagents to complete the given reaction.

A: Reaction 1 : At ring junction methyl and hydrogen are trans. In the product Me and H are opposite…

Q: CI H30* Choose. ?

A: We have to predict the, product of the given reaction.

Q: Complete the synthesis below, including all reagents and intermediate products. You don't have to…

A: The reaction in which cyclic adduct is formed by the combination of two or more unsaturated molecule…

Q: Show how to convert the given starting material into the desired product. Note that some syntheses…

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Q: pCH;C,H,SO,Cl NaBr tosylate base ethanol CH3

A: The reaction occurs through SN2 mechanism.

Q: OH OH 7. 8. 9.

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Q: Question attached

A: In an organic reaction, a nucleophile attacks an electrophile.

Q: Draw the major product of the following reaction sequence. OH H2CrO4 HO NaBH4 H*/H20 ELOH он H3C* но

A: Explanation step wise .

Q: Heat Benzaldehyde + KCN + EtOH

A: Concept introduction: Benzoin condensation: It is the coupling reaction that is occur between the…

Q: accomplish

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Q: Draw the major product for each reaction. HNO3 H,SO4 O,N fuming H,SO4 NO2 OMe CI AICI3

A: Note: As per company norms we can answer only 3 subparts. Please share rest of the parts as a…

Q: draw the product

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Q: 2. Give a stepwise mechanism for each reaction (i) OH 1) CH;MgBr (excess) 2) H2О (ii) OCH3 „NO2 N-…

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Q: Perform the following transformation and propose a mechanism Br ОН Br НО

A: When alpha-bromo ketone reacts with NaOH then to get carboxylic acid is formed. This is called…

Q: 20. (10 points) Predict the product and draw the curved arrow mechanism for the transformation…

A: In the given question we have to solve the epoxide ring opening in the presence of LiAlH4 and water,…

Q: 2 Li CH3B1 H3o+ ?

A: Organolithium reactants attack electrophillic Carbon atoms which are there in Carbonyl compounds and…

Q: *NH H*

A: Reactants are secondary amine and ketone, medium of reaction is acidic medium.

Q: Which reaction does not correctly circle the more stable base? A) + CH3 B) + OCH3 OCH3 C) Но + H20 +…

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Q: Match each reaction sequence to a product below. Assume any necessary workup. Answers may be…

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Q: Br NaOH heat Draw E1 Major Product + Draw Minor E1 Product

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Q: Propose a mechanism for each of the following reactions: OH Hgo"

A: The alkene undergoes hydrolysis reaction in presence of H3O+ to give the hydrolysed product,…

Q: Draw a curved arrow mechanism and predict the product. H EN CH3 H3C Create OscerSketch Answer 1…

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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.