1. Consider the following reaction: CL2 CH4 -----> Hv (a) Predict products and write complete chemical equation: (b) Write a stepwise mechanism for monochlorinated product formation. Be sure to show all the intermediate structure and all the electron flow using arrows.
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.
1. Consider the following reaction:
CL2
CH4 ----->
Hv
(a) Predict products and write complete chemical equation:
(b) Write a stepwise mechanism for monochlorinated product formation. Be sure to show all the intermediate structure and all the electron flow using arrows.
- Consider the following reaction:
Br2
CH3CH=CH2--------->
(a) Predict products and provide complete equation
(b) Write a stepwise mechanism. Be sure to show all the intermediate structure and all the electron flow using arrows
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- Consider the following reaction:
Br2
CH3CH=CH2--------->
(a) Predict products and provide complete equation
(b) Write a stepwise mechanism. Be sure to show all the intermediate structure and all the electron flow using arrows
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