The follow ing compound can be synthesized by a mixed Claisen condensation. Identify the two compounds that give this condensation product. and HO and B. and and A MacBook Pro

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

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Q: C NasH Hgot

A:

Q: The

A: We will write the reason of difference in reactivity

Q: Provide the Cruved arrow mechanism of anisole treated with bromine with iron (III) bromide. Include…

A: Here we are required to predict the mechanism of anisole with bromine with FeBr3.

Q: Devise a synthesis of attached compound from the indicated starting material.

A: The synthesis of given compound from the indicated starting material can be shown as follows,

Q: Which of following ethers cannot be made by a Williamson ether synthesis?

A: Williamson ether synthesis involves the reaction of alkoxide ion with primary alkyl halide. This is…

Q: (−)-Hyoscyamine, an optically active drug used to treat gastrointestinal disorders, is isolated from…

A: (a) (-)-Hyoscyamine contains two hydrogens which are acidic, which are benzylic and alcoholic…

Q: (A) Provide the major organic product for the reaction below (B) Would the product be optically…

A: Sugar undergoes oxidation reaction in presence of HNO3 . Both aldehyde and alcohol group is oxidis

Q: c. Describe (using appropriate figures) one reaction that exploits epoxides as the starting…

A:

Q: 3. Draw a detailed arrow pushing mechanism for the following reaction H i. Og, ii. PPH3 CH2CI2 H

A:

Q: Can you help propose a sy

A: 1. Cyclohexane is converted in to cyclo-1,3-hexadiene :  cyclohexane upon treated with chlorine…

Q: Which reagents could be combined to make the following in a reasonable number of steps and order?

A: To determine which reagents could be combined to make below compound

Q: Provide a note on Peterson syntheses, with suitable example and mechanism.

A: Peterson synthesis is synthesis of olefinic double bond from carbonyl using α-silyl alkane.

Q: Draw the mechanism with curved arrows (Williamson Ether Synthesis). Please provide detailed…

A: Williamson synthesized the ether from alcohol

Q: What would be an appropriate term to describe molecules B and C? in A В Me `Me Me resonance…

A: Molecule A is conjugated. B and C are skip diene

Q: Is a intramolecular Friedel Crafts acylation reaction. As you from the product, the acylation…

A: Applying concept of organic synthesis and reagent.

Q: B A OH Compound A can be converted to cyclobutanol using the reagent Compound B can be converted to…

A: Organic chemistry in which we deal with organic reactions which covert organic reactant in to…

Q: Question are attached

A: In question 1 structure b) contains more acidic H-atom .because after the removal of that H-atom the…

Q: Pentalene is most elusive molecule and has never been isolated. The pentalene dianion, however, is…

A: Aromatic Compounds are the compounds which are planar, cyclic, conjugation of π electrons and has to…

Q: The saccharide shown here is present in some plant-derived foods.            (a) Indicate the…

A: Given saccharide structure is:

Q: Explain why compound A does not undergo an E2 elimination with strong base.

A: For the structure to be more stable it has to have the bulky phenyl group in the equtorial position.…

Q: Draw the major product(s) of nitration of benzoic acid.

A:

Q: How many singlets in will be observed in the ¹H NMR spectrum of this compound? od

A: NMR spectroscopy is nuclear magnetic resonance spectroscopy

Q: Provide mechanism with curved arrows for Part B: Synthesis of benzil

A: PhC(=O)-CH(IH)-Ph on oxidation with HNO3 gives Ph-C(=O)-C(=O)-Ph which is called benzil.  At first…

Q: Devise a stepwise synthesis of attached compound from dicyclopentadiene using a Diels–Alder reaction…

A: Our target molecule is

Q: он Synthesize the compound in 2 different ways using Grignard reagents and reactions

A: In the organic synthesis, suitable reagent converts the reactant into products. Reagents attacks…

Q: What starting materials are needed to synthesize each attached compound by a Robinson annulation?

A: Robinson Annulation is an organic reaction that takes place between alpha-beta unsaturated carbonyl…

Q: a) What is (are) the major product(s) of the nitration reaction. Explain this selectivity, and…

A:

Q: provide CLEAR AND NEAT mechanism with curved arrows for  Part A: Synthesis of benzoin

A: At first HO^- abstract the most active hydrogen from thiamine hydrochloride to get nucleophilic…

Q: C. Using any necessary reagents of 2 carbons or less, and any other necessary inorganic reagents,…

A: The synthesis of the given compound is given below.

Q: 7. Propose an efficient synthesis of for each of the following transformation: a) b)

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Q: Which of the following requires a tert-butanol as one of the reactants in Williamson ether…

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Q: (−)-Hyoscyamine, an optically active drug used to treat gastrointestinal disorders, is isolated from…

A: (a) (-)-Hyoscyamine contains two hydrogens which are acidic, which are benzylic and alcoholic…

Q: reasonable synthesis? might need to use both grignard and a gilman reagent (organocuprate)

A: Synthesis of product by using Gilmann and Grignard reagent.

Q: Perform a retrosynthetic analysis (please include - disconnection etc) and suggest a synthesis of…

A: The retrosynthesis method is used to determine the starting material by the fragmentation of the…

Q: From the given starting material provide a reasonable synthetic route to the following plecule. O,N.

A: Here we have to prepare the given compound from the starting material 2-methylbuta-1,3-diene in…

Q: base ? A B

A:

Q: Two of the following will give the same dimethylcyclooctatriene prod (A) while the third one will…

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Q: Provide a retrosynthetic analysis and forward synthesis for the compound shown below. and any other…

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Q: Provide mechanism with curved arrows for Part C: Synthesis of tetraphenylcyclopentadienone

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Q: With this in mind, draw the product when each compound undergoes anintramolecular Diels–Alder…

A: Diels Alder reaction is [4+2] cycloaddition reaction. It is reaction between diene and dienophile…

Q: You have learned two ways to make an alkyl benzene: Friedel–Crafts alkylation, and Friedel–Crafts…

A: The general mechanism for Friedel-craft’s alkylation is given below\ where R is alkyl group

Q: Propose an efficient synthesis of the following molecules. I.

A: 1- First we need to identify the starting material so we will do retro-synthesis for this given…

Q: Is UV spectroscopy a correct method to distinguish between the Rectant and Product

A: UV Spectroscopy Absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible…

Q: Provide a curved arrow mechanism for the SN1 reaction below: CI CH3 H,C NACN

A: SN1 is a unimolecular nucleophilic substitution reaction. A carbocation is formed after the eviction…

Q: Make an electron-flow-mechanism for this synthetic scheme. This involves predicting major and by.…

A: Solution -

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: The plausible arrow pushing reaction mechanism is provided below in attach image .

Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.