Row A. B. C. D. Use the following information to answer question 24. A Model of an Organic Molecule Row IUPAC Name 2-methylbutan-3-ol 2-methylbutan-3-ol 3-methylbutan-2-ol 3-methylbutan-2-ol 24. For the organic molecule represented by the model above, which of the following rows identifies its IUPAC name and a possible isomer? Isomer pentan-1-ol cyclopentanol pentan-1-ol cyclopentanol Common Classification Legend Property of C₂H4(g) Incoturated Hydrogen 25. Which of the following rows identifies the common classification of C₂H4(g) and C₂H4Cl₂(g), and identifies properties that distinguish them from each other? Property of C₂H4Cl₂(g) Saturated Carbon Oxygen

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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.