4. Devise a forward synthesis given the retrosynthetic analysis, only using the starting materials given and employing only Suzuki reactions for C-C bond forming reactions. || Br CH,0 CH,O |

Q: Show the mechanism (arrow pushing) for the following reaction: 1. NANH2 2. Br

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Q: 1. For the transformation below, provide a detailed arrow-pushing mechanism. If intermediates occur…

A: The given substrate to you, has a acidic hydrogen and a good leaving group -OEt. Thus to find the…

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A: Given reaction is interanolecular reaction

Q: 3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents…

A: Benzene on F.C.Alkylation to form Methyl benzene (Toluene) in first step. Then Toluene undergoes…

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Q: 4. A student performed the following sequence of reactions: an oxetane opening, followed by a…

A: As per the given data, 1 H- 1.25 3H t 1.28 6H s 1.65 2H t 2.60 2H t 3.45 2H t 7.2- 7.3…

Q: O Br Br O OMe NH₂

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Q: Draw a plausible arrow pushing mechanism for the reaction below. You must use the exact structures…

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Q: 16. Provide a curved arrow mechanism for the transformation shown below. Be sure to show the…

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Q: 4) Provide a list of reversible vs irreversible carbonyl additions.

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Q: 2.Provide the most probable reagent(s) to accomplish the following reaction: HO

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Q: Predict the mechanism of the rection below.

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: synthesis. the letters of the reagents in the order that they are used; example: fa. Reagents…

A: Given : We have to write the reagent and prepare the given product from benzene.

Q: OH (TM) (CH₂)4CH3 (SM) H

A: Here we have to synthesize the following given target compound from the given starting material by…

Q: 6. When the following transformation was conducted at an appropriate temperature, the following two…

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Q: propose a synthetic route to this structure that includes at least one C-C bond formation step.

A: 2 -Methylbutanoyl chloride can be synthesized as given below.

Q: OH The transformation above can be performed with some reagent or combination of the reagents listed…

A: The major steps involved in this reaction are hydroboration to give alcohol, oxidation by mild…

Q: In the box, provide structure of the product for each transformation reaction below. Ph-H…

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Q: c) Outline a synthesis for compound G shown below starting with a 2- hydroxybenzylketone.

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Q: он The transformation above can be performed with some reagent or combination of the reagents listed…

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Q: When an electrophilic aromatic substitution reaction on naphthalene is reversible, such as in a…

A: The major product of the reaction has to be given,

Q: With reference to the following reaction scheme: LIAIH4 Et,NH HCI (cat.) A C3H180 B C12H25N Me Но…

A: We have to draw the structures of the compounds A-D.

Q: For question 1a and 1b below, which of the puzzle pieces makes the best sequence for each synthesis?…

A: 1. In presence of bulkier base like teritiarybutoxide Hofman elimination takesplace , less…

Q: 1. BH3 THF 2. H₂O2/NaOH/H₂O ●

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Q: For the transformation shown, select the most appropriate reagent(s) to effect the change, ?? H. 1)…

A: The reaction is the Ozonolysis  Reagent : (1) O3  , (2) DMS (dimethyl sulphide) This is called…

Q: H2O, H2SO4 H9SO4 A. В. С. E. None of these choices is correct. D.

A: In presence of HgSO4 and H2SO4 , H2O ,oxymercuration-demercuration reaction is carried out and…

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, Sn2, E1, and/or E2 (write…

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Q: The following transformation can be accomplished by using. to make the product. 1) Br2, FeBr3 2)…

A: -> Aromatic compound can give electrophilic aromatic substitution reaction by replacing hydrogen…

Q: 2. A chemist wishes to perform the nitration of methyl benzoate as follows: HNO3, H2SO4 Draw a…

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Q: the given compounds. Write your answers on the space/field provided. Separate the reagents with a…

A: The answer is as follows:

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, SN2, E1, and/or E2 (write…

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Q: 2) Write a detailed mechanism for the following reaction: H2SO4 CH;CH,C=CH + H2O CH;CH,CCH3

A: Hydration reaction of Alkyne takes place in acidic medium as follows:

Q: Choose the best reagent (A-Ej for carrying out the following conversion from the list provided below

A: Given: structure of reactant and products Nabh4 doesn't reduce acid group

Q: How would you synthesize the following compounds from butanoic acid using reagents from the table?…

A: LiAlH4 is a reducing agent which reduces acid to alcohol.

Q: Propose a feasable synthesis of the target molecule (TM, Fig. 1) from the indicated starting…

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Q: CI OH

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Q: 6. When the following transformation was conducted at an appropriate temperature, the following two…

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Q: 3. Provide full mechanism (curved arrows and intermediates) for the following reaction. OCH3 1.…

A: Answer 3 )  The mechanism for the given reaction = ?  Note : As per our company guidelines, we are…

Q: Determine the structures of compounds A-J in the following reaction sequences. 1. LIAIH4, ether В 2.…

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Q: 3) Design a reasonable synthesis for the following transformation. = trort + B.

A: Here we have synthesize the given polymer which is a polyester obtained from starting material…

Q: 4. Provide the major organic product (elimination rxn): NAOCH. CH;OH Br a. CH3 nCH3 NaOH Br b. КОН,…

A: Since, you have asked multiple question, we will solve the first question for you. If you want any…

Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. I1,0

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Q: Provide the reagents necessary to complete the following transformation. CH, -CH3 to

A: free-radical halogenation (more substituted alkyl halide is formed) E1 elimination  acid catalyzed…

Q: Given the reaction below Me" Me Br₂ H₂O a. Provide the product(s) from the reaction, and if multiple…

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Q: -CH, CH, HyC

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Q: Br Mg ? →? H

A: The given reactant is Bromo benzene.

Q: Provide the appropriate reagent(s) and conditions for the following transforma ベロで NH2 Ph Ph Ph Ph.

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Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

A: The given reaction is diazotisation reaction. In this reaction a diazonium salt is formed as a…

Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

A: Applying basic rule of reagents and chemical reaction.

Q: mCРВА О ČI

A: