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In acids, the electron-releasing inductive effect of the alkyl group increases the electron density on oxygen and thus hinders the breaking of the O-H bond, which consequently reduces the ionization. Due to its greater ionization, formic acid ( pK a =3.74 ) is stronger than acetic acid ( pK a =4.76 ).
Because inductive effects depends strongly on proximity, the meta and ortho positions of fluorobenzene are considerably less reactive than benzene. Thus, electrophilic aromatic substitution on fluorobenzene is strongly para selective. This -I and +M effect is true for all halides - there is some electron withdrawing and donating character of each.
Alkyl groups are electron donating by inductive effect, and increase the electron density on the sigma bond of the alkene. Also, alkyl groups are sterically large, and are most stable when they are far away from each other. In an alkane, the maximum separation is that of the tetrahedral bond angle, 109.5°. In an alkene, the bond angle ...
Amine alkylation (amino-dehalogenation) is a type of organic reaction between an alkyl halide and ammonia or an amine. [1] The reaction is called nucleophilic aliphatic substitution (of the halide), and the reaction product is a higher substituted amine. The method is widely used in the laboratory, but less so industrially, where alcohols are ...
In order for the S N 2 reaction to take place there must be a good leaving group which is strongly electronegative, commonly a halide. [4] In the Williamson ether reaction there is an alkoxide ion (RO −) which acts as the nucleophile, attacking the electrophilic carbon with the leaving group, which in most cases is an alkyl tosylate or an ...
Sir Christopher Kelk Ingold BEM FRS [1] (28 October 1893 – 8 December 1970) was a British chemist based in Leeds and London. His groundbreaking work in the 1920s and 1930s on reaction mechanisms and the electronic structure of organic compounds was responsible for the introduction into mainstream chemistry of concepts such as nucleophile, electrophile, inductive and resonance effects, and ...
However, one way inductive effects of functional groups can be investigated is by probing b-substituent effects where the heteroatom would be a methylene group away from the vinyl cation (-CH 2 Y). In –CH 2 Y groups that exhibit a very small or no p donation, there is only a very small difference in the hyperconjugative effect in the –CH 2 ...
The scope of the Corey-House synthesis is exceptionally broad, and a range of lithium diorganylcuprates (R 2 CuLi, R = 1°, 2°, or 3° alkyl, aryl, or alkenyl) and organyl (pseudo)halides (RX, R = methyl, benzylic, allylic, 1°, or cyclic 2° alkyl, aryl, or alkenyl and X = Br, I, OTs, or OTf; X = Cl is marginal) will undergo coupling as the nucleophilic and electrophilic coupling partners ...