Using the reagents below, list in order (by letter, no period) those necessary to transform toluene into assume any undesired regioisomers can be separated. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. A.H₂, Pd B. i.KMnO4, OH", ii.H3O+ C. CH3COCI, AICI 3 D. Zn(Hg), HCl, reflux E. i.O3, H₂O ii. Zn, H₂O F. MMPP,CH3CH₂OH G. i. BH3; ii. H₂O2, NaOH L.HCI, peroxide M. SOCI₂ N. Br2, FeBr 3 O. Cl₂, hv P. Cl2, FeCl3 Q. H₂O, H₂SO4 R. CH3CH₂CH₂CI, AICI3 Br OH. You may
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.
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