Which of the following statements about an SN1 reaction is true? A. the reaction occurs in one-step B. there is no effect on reaction rate by nucleophile C. primary alkyl halides react faster than secondary alkyl halides D. the reaction proceeds with inversion of stereochemistry E. the reaction is favored by aprotic solvents
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.
![Which of the following statements about an SN1 reaction is true?
A. the reaction occurs in one-step
B. there is no effect on reaction rate by nucleophile
C. primary alkyl halides react faster than secondary alkyl halides
D. the reaction proceeds with inversion of stereochemistry
E. the reaction is favored by aprotic solvents](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc0556e3f-f93e-45fb-ae95-3c114a64e60e%2F29f9e4e0-d8e3-42b9-afc4-2682b5e7a298%2Fuj1rp_processed.png&w=3840&q=75)
![Which of the following statements about an SN2 reaction is true?
A. There are two transition states.
B. There is one energy maximum.
C. The transition state can be isolated and studied.
D. For a carbon electrophile in the transition state, the hybridization of an sp3
carbon remains unchanged.
E. The reaction rate does not depend on the concentration of the electrophile.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc0556e3f-f93e-45fb-ae95-3c114a64e60e%2F29f9e4e0-d8e3-42b9-afc4-2682b5e7a298%2Fpjn3e1j_processed.png&w=3840&q=75)
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