Using the Grignard reaction, NBS, NaCN and any other reagents, synthesize Phenylacetone from Toluene, You can use any other reagents necessary. List all the reagents and conditions needed in each step to account For the formation of the product(s).

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A: Please find the attachment.

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Q: QUESTION 7 A compound of molecular formula C9H1203 has two strong infrared absorptions between 1100…

A: Spectroscopic techniques are used to identfy structure of chemical compound

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Q: 00 80 60 40 20 0 20 40 60 80 1

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Q: 3. Describe the formation of dative covalent bond using NH4* as example.

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Q: 3. Name each compound according to the IUPAC system.

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Q: Hypothetically, what would be the conjugate acid of H3O+

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A: Chemical kinetics is branch of chemistry that deals with rates of chemical reactions.

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Q: 1. Which compounds can exist as cis-trans isomers? Draw them. CH2=CHCH,CH, CH3 CH3CH=CHCH₂CH3…

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Q: 11. The amine below can be prepared from the ketone shown and what reagents? i ? (A) 1. NaCN 2.…

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Q: E) LOCH3 1. AlCl3 2. H20

A: This is an example of friedel Craft acylation reaction in which anhydride react with lewis acid .

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.