Q4: Give the major organic product(s) of the following reactions CH₂OH PCC CH₂Cl₂ KMnO4 MgBr NBS light 1. ether 2. H₂0*

Q: Change the bond between the two carbon atoms in each molecule to a double or triple bond as needed…

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Q: (c) OH alcohol * II.. 1. SOC12 2. 1 equiv. NaOEt 3. Br2 4. 2 equiv. NaNH2/NH3 5. H₂/Lindlar Sn ?…

A: 1) SOCl2 Converts alcohol OH into alkyl chloride Cl2) NaOEt Acts as a base and undergoes elimination…

Q: please explain part d in detail

A: Acid is a molecule that loses its proton (H+) easily.More readily the proton is lost, most acidic…

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A: Ka of HNO2 = 4.0 × 10-4 NO2- is the conjugate base of HNO2

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A: Steriochemistry  It is the study of arrangements of atoms in the Molecule . By the studing the…

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Q: OH Hint: can be accomplished in 3 steps.

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A: According to the answering guidelines, I'm posting the solution for the first question. Kindly post…

Q: a OH alcohol 1. SOC1₂ 2. 1 equiv. NaOEt 3. Br2 4. 2 equiv. NaNH2/NH3 5. H₂/Lindlar

A: SOCl2 ..... Converts OH to Cl NaOEt ..... Acts as a base  Br2 ...... Adds to the double bond NaNH2…

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Q: See Figure 3-1. Which structures are identical to Compound 1? A B C D

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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.