kk. ethyl dimethylamine + H2O2 in DMSO Reaction Type(s) Mechanism(s) CH3 -N-CH2 - CH3 CHy Product(s). Stereochemistry (if applicable)

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A: Given incomplete reaction is :  CH3CHBrCH3 + NaOCH3 in methanol ---------------> ?  Given the…

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A: The answer is given as follows

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Q: Write whether it will be E1, E2, SN1, and/or SN2 Show the mechanism(s) Write the MAJOR product(s)…

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A: The reaction mechanism is given below -

Q: ОН О MECN OMe OMe H2SO4 NHAC

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A: epoxide are electrophilic in nature so it undergo nucleophilic substitution reaction

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A: It is SN1 type reaction.

Q: 1) Cl2, H30* 2) NaCN 3) H2SO4, H20 4) SOCIl,

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Q: uu. 3,3-dimethylbutan-2-ol + H:PO4 in water Reaction Type(s) Mechanism(s) CH3 CHy- CH-ċ-CH3 OH CH3…

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Q: vv. 2-chloro-2-methylpropane + NaOH in CH;Cl2 Reaction Type(s) Mechanism(s) CH3 c - CI CH3

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Q: 2. For each of the following reactions or series of reactions, indicate the starting material,…

A: These are addition reactions and chlorination reactions.

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Q: k. (R)-3-methylbutan-2-ol + TsCl + pyridine in DMSO Reaction Type(s) Mechanism(s) CH3 CHy-cH-CH -CH3…

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A: Heterocyclic compounds: The organic molecules/compounds which contain an atom other than carbon and…

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Q: gg. 3,3-dimethylbutan-2-ol + concentrated HCl in water Reaction Type(s) Mechanism(s) CH CH3- CH - C-…

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Q: product(s) type of reactlon DMSO Nal acetone но

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A: Given incomplete reaction diagram is : Complete the reaction diagram =  ?

Q: Consider the following statement  in reference to SN1, SN2, E1, and E2 reactions of haloalkanes. To…

A: Given statement: Substitution at a stereo center gives predominantly a racemic product.

Q: dd. 2-bromo-2-methylbutane + H2O Reaction Type(s) Mechanism(s) CH3 CH3 -CH2- - CH3 Br Product(s).…

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Q: OH 1) ТBDMSCI 2) а. NaCCCHg b. Hзо* H,C 3) H2. Pd/C 4) BUANF, THE

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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.