explain IR data and any information discern from it. This IR is a product of Benzophenone reaction which is Diphenylmethanol

Q: methylbenzene with propanoyl chloride and AIICI3 to make `CH2-CH3 H3C

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Q: Based on the image attached, explain the step-by-step mechanism reaction of reduction for…

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Q: The molecule below will produce a positive test with OCH3

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Q: Friedel-Crafts alkylation can be difficult to control. What are some of the experimental methods…

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Q: CI но. он HO,

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Q: Lewis Acid

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Q: "NH₂ NH₂ CH₂Br DMF CH₂Br (excess)? DMF ?

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Q: GENERAL SCHEME PDL2 R-X + R'B(OR),- R-R

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Q: label the Product Benzophenone Reaction spectra and peaks and explain why each peak is that

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Q: i) Give the IUPAC name of this molecule. ii) Outline the mechanism of this reaction. Your mechanism…

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Q: Why is this Beckmann rearrangemnt useful for the synthesis of acetaminophen?

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

Q: Please help! And what is the direction of the molecular dipole moment in the chloroform molecule?…

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Q: Provide the missing reagent to complete the following reaction. CH,CH,CH,ONa ? Write your answer on…

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Q: What simple characterization techniques can you say that your product is dibenzalacetone?

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Q: b) A key piece in the synthesis is the molecule below. Provide a reaction that makes this piece that…

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Q: Discuss the truth of the following statement. Explain why it is true or false Every SN1 reaction…

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Q: How can this transformation be carried out using only heat or light?

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Q: According to the IR spectrum what is the major product of the reaction sequence shown in the box?…

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Q: Look up the model that is used to predict stereochemical outcome of Sharpless asymmetric…

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

Q: Draw the structure of 2-bromo-4-methylaniline in the window below.

A: Here we are required to structure of 2-bromo-4-methylaniline.

Q: stereogenic centers

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Q: This

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Q: Using the nomenclature guide, provide an appropriate name for the following molecule. Me Me

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Q: Cyanohydrin formation is useful because of the further chemistry that can be carried out on

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Q: Draw geometrically clear picture of the most stable enol form of the compound shown below, and point…

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Q: How will you distinguish the following pairs of compounds by UV spectroscopy? (Hint: Calculate the…

A: To distinguish between the given compound by observing UV spectroscopy:

Q: Explain the benzyne mechanism.

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Q: What is mechanism of ether cleavage  Is this cleavage following SN1 or SN2 ? Give your explanation

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Q: 1. NaOCH3 2. Br- Br 3. NaOCH3 4. LIAIHĄ 5. Н.О 6. , H3O* (cat.)

A: Dimethyl malonate reacts with base.

Q: Can you please send me the answers for d) and e) attached.  Thanks. Are the following molecules…

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Q: Determine the product of the reaction

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Q: OCH LOCH

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Q: menthol он он OH OH HO, A в D E

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Q: By giving the reagent and the visible result, differentiate each of the following pairs

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Q: Thiatriazoles, when heated de-compose vigorously. Why is this?

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Q: 4. Which do you think is more chemically stable, the reactants or products of each of the reactions…

A: As all the above process result in production of energy it means all reaction are exothermic.

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.