10. Under acidic conditions, both ketones shown below can tautomerize to the enol. For one of the ketones below, tautomerization to the enol is considerably more favorable than for the other. A Draw the enol tautomer for each, and explain which ketone you would expect to form a larger quantity of the enol tautomer in three sentences or less. H3O+/H₂O Explanation: Enol A H₂O+/H₂O Enol B
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.
Step by step
Solved in 3 steps with 3 images
