A-Hydrogen atom

Phenols formed by the substitution of a hydrogen atom by a hydroxyl group, OH, in an aromatic ring ( I t)... 

Some of the common aromatics found in crude oil are the simple derivatives of benzene in which one or more alkyl groups (CHg) are attached to the basic benzene molecule as a side chain which takes the place of a hydrogen atom. These arenes are either liquids or solids under standard conditions. 

The energies of transitions of a hydrogen atom starting from the ground state fit exactly the equation... 

BUTENE. As shown in Figure 38, a group attached to C-1 can migrate from position 1 to 3 (1,3 shift) to produce an isomer. If it is a methyl group, we recover a 1-butene. If it is a hydrogen atom, 2-butene is obtained. A third possible product is the cyclopropane derivative. The photochemical rearrangement of 1-butene was studied extensively both experimentally [88]... 

In a photochemical experiment, irradiation of benzene leads to Sj, which connects to the ground-state surface via the conical intersection shown. Benzene, the much more stable species, is expected to be recovered preferentially, but the prebenzvalene structure which hansfomis to benzvalene is also fomied. Another possible route from the prebenzvalene, along a different coordinate, will lead to fulvene [90, p.357] after a hydrogen-atom transfer from... 

Table 7-1 lists some comparisons between experimental mean molecular polarizabilities and those estimated by Eq. (6). In this scheme, the estimation of mean molecular polarizability for acetic add needs five values, values for sp -C, for sp -C, for sp -O, for sp -O, and for a hydrogen atom. 

Brominarion of the aromatic nucleus is now regarded as replacement of a hydrogen atom of the intact nucleus as a result of an attack by a polarised complex with a positive end. Iron acts as a carrier by forming FcBrj, which as a Lewis acid forms a polarised complex with one mol. of Bri ... 

The hamionic oscillator (Fig. 4-1) is an idealized model of the simple mechanical system of a moving mass connected to a wall by a spring. Oirr interest is in ver y small masses (atoms). The harmonic oscillator might be used to model a hydrogen atom connected to a large molecule by a single bond. The large molecule is so... 

Only esters containing two a-hydrogen atoms (ethyl acetate, propionate, n-butyrate, etc.) can be condensed with the aid of sodium alkoxides. For esters with one a-hydrogen atom, such as ethyl tsobutyrate, the more powerful base sodium triphenylmethide PhaC Na leads to condensation with the formation of ethyl a-tsobutyrylisobutyrate ... 

The acetoacetic ester condensation (involving the acylation of an ester by an ester) is a special case of a more general reaction term the Claisen condensation. The latter is the condensation between a carboxylic ester and an ester (or ketone or nitrile) containing an a-hydrogen atom in the presence of a base (sodium, sodium alkoxide, sodamide, sodium triphenylmethide, etc.). If R—H is the compound containing the a- or active hydrogen atom, the Claisen condensation may be written ... 

Alternatively, it may bo assumed that the basic ethoxide ion attacks a hydrogen atom of the activated CH, group to yield the carbanion directly ... 

Malonic ester, like acetoacetic ester (Section 111,151), when treated with an equivalent of sodium ethoxide, forms a mono-sodium derivative, which is of great value in synthetical work. The simplest formulation of the reaction is to r rd it as an attack of the basic ethoxide ion on a hydrogen atom in the CH, group the hydrogen atoms in the CHj group are activated by the presence of the two adjacent carbethoxyl groups ... 

Here the phenylacetic anhydride, possessing more reactive a-hydrogen atoms, condenses with benzaldehyde to give a-phenylcinnamic acid. The preparation of the latter is an example of the Oglialoro modiflcation of the Perkin reaction. 

A ketone having an a-hydrogen atom may be acylated with an eater or an acid anhydride to form a p diketone ... 

Removal of an a-hydrogen atom of the ketone as a proton to form n carbauion (acetone anion) ... 

Aromatic aldehydes, and also aliphatic aldehydes containing no a-hydrogen atom, undergo the Cannizzaro reaction (see Section IV,123) when treated with aqueous alkali, for example ... 

To sum up, spectroscopic data indicate the amino" form (10) is predominant when R is a hydrogen atom or an alkyl group, while the imino form (11) is predominant when R is an aryl group (Scheme 66). 

Benzoyl peroxide has been the most common source of phenyl radicals. But in reaction with thiazoles the benzoyloxy radical abstracts a hydrogen atom from the thiazole nucleus or from a methyl group in the case of methylthiazoles, giving by-products such as dithiazolyls or 2.2 -dithiazolylethane (183). The results obtained with benzoyl peroxide are summarized in Tables III-23, III-24. and III-25. 

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