Tolyl

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In organic chemistry , tolyl groups are functional groups related to toluene. Tolyl groups are aryl groups which are commonly found in the structure of diverse chemical compounds. They are considered nonpolar and hydrophobic groups. The functionalization to include tolyl groups into compounds is often done by Williamson etherification , using tolyl alcohols as reagents, or by C-C coupling reactions. Tolyl sulfonates are excellent leaving groups in nucleophilic substitutions , for this reason, they are commonly generated as intermediaries to activate alcohols. To this end, 4-toluenesulfonyl chloride is reacted in the presence of a base with the corresponding alcohol. This organic chemistry article is a stub.

Tolyl

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The syntheses, spectroscopic characteristics, and electrochemical behavior of 1,1-dimethyl-2,5-diphenyl-3,4-bis p -methylphenyl silole and 1,1-dimethyl-2,3,4,5-tetra p -methylphenyl silole are reported. The compounds are weakly luminescent in dilute fluid solution but exhibit dramatic aggregation-induced emission AIE. Absorbance, luminescence, and voltammetric characteristics are compared to 1,1-dimethyl-2,3,4,5-tetraphenylsilole and 1,1-dimethyl-3,4-diphenyl-2,5-bis p -methylphenyl silole, allowing a comparison of the effects of the position of the substituents on the silole ring. Substitution of the weakly electron-donating p -methyl groups on the peripheral aryl groups at the 2- and 5-positions of the silole ring results in slight red shifts in absorption and emission maxima, slight enhancement of luminescence quantum yields, slightly longer luminescence lifetimes, and more anodic oxidation potentials. This is a preview of subscription content, log in via an institution to check access. Rent this article via DeepDyve. Institutional subscriptions. Adachi, H.

Tolyl

In organic chemistry , tolyl groups are functional groups related to toluene. Tolyl groups are aryl groups which are commonly found in the structure of diverse chemical compounds. They are considered nonpolar and hydrophobic groups. The functionalization to include tolyl groups into compounds is often done by Williamson etherification , using tolyl alcohols as reagents, or by C-C coupling reactions. Tolyl sulfonates are excellent leaving groups in nucleophilic substitutions , for this reason, they are commonly generated as intermediaries to activate alcohols.

Kjv numbers 6 24 26

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The para orientation illustrated p -toluenesulfonyl is most common, and by convention tosyl without a prefix refers to the p -toluenesulfonyl group. For S N 2 reactions , alkyl alcohols can also be converted to alkyl tosylates, often through addition of tosyl chloride.

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