Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. 1) PhMgCl (C6HsMgCl) 2) HCI/H₂O HO O H 'Н Please select a drawing or reagent from the question area
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.
Please help solve. There are two products to draw, I attempted them as shown but they are incorrect.
- Grignard reagents have the general form of RMgX, where R is an alkyl or phenyl.
- It is an important source of nucleophilic carbon.
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Thank you for the answer! However, in Aktiv Chemistry it's not giving me the option to put the Ph. Would putting Br where the Ph is be the same? Thank you for your contiued help.
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