Draw the starting reactant that would produce this alcohol when treated with this reagent. Ignore inorganic byproducts. Select to Draw 1. NaBH4 2. H3O+ OH

Q: 44 H- H I I +4 H- -H I H H + H H -0-H I tr H -H ·0-H alcohol carboxylic acid amine aldehyde ketone

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Q: are they: secondary, primary, tertiary  or phenol alcohol?

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Q: 3. Name this ether correctly. NO₂ (0) -OCH₂CH3

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Q: Which of the following reagents converts an alcohol to an alkoxide? NaH HC1 Mg(OH)2 H₂SO4

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Q: C H* CH,CH,CH,OH H,C OH С - ОН H* CH,CH,OH H* CH,CH,CH,OH CH,CH,COOH

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Q: 4) A reagent that can reduce a carboxylic acid to an alcohol is A) H2/Pt B) K2Cr207 C) NaBH4 D)…

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A: Dear student I have given answer to your question in the image format.

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Q: 2. Draw the following molecules 2,4-dimethyl-2-pentanol 2,3-dimethyl-1-butene 3-ethyl-2-hexanol…

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Q: CH- CH OH -> )CHy-CHCH-CH2 CH-CH-CH d) Cig-CーCH-CHy OH OH e) CH ーぎ

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Q: What is the IUPAC name of the following compound? Br CH3 H3C A. 5-Bromo-2-methylphenyl ethanoate B.…

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Q: ОН CH3

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Q: Write the IUPAC names for these alcohols. a. но но

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Q: what are the IUPAC names of the alcohols that could be used to produce this compund?

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Q: СООН

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Q: CH2 CH3 OH hemiacetal acetal neither CH3—O—CH—O CH3 CH3 hemiacetal acetal neither

A: Thank you.

Q: 1. Name the following carboxylic acids. Use both IUPAC and common names. H- C-OH ) CHz-CHz-COOH

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Q: Give the systematic (IUPAC) names for these molecules. Boononon cnolonongron. НаСНз CHОССH2СH2СНCHЗ…

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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.