Zobrazeno 1 - 6
of 6
pro vyhledávání: '"F. S. Dubnikova"'
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:1173-1176
1. Various paths for the reaction of acetylene with the hydroxide ion have been evaluated with the aid of quantum-chemical calculations, and it has been shown that the formation of the acetylide ion (HC≡C−) is the preferable direction. 2. The for
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 38:1645-1648
A stepwise mechanism for the formation of benzene as a secondary product of a nucleophilic addition reaction to acetylene in media with increased basicity has been proposed. The cyclotrimerization of acetylene takes place as a result of the successiv
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:1841-1846
1. The predominant direction of the reaction of acetylene with a molecule of lithium hydroxide in both the dissociated and undissociated states is the formation of the molecular π complex C2H2· LiOH. 2. The formation of the complex C2H2· LiOH is a
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:1177-1180
1. According to the data form quantum-chemical calculations, the formation of vinyloxy anions from acetylene molecules and hydroxide ions occurs with the intermediate participation of [HC=CHOH]− anions (cis or trans), whose further conversion is po
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 38:1641-1645
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:1180-1182
1. According to the data from the quantum-chemical calculation, the vinylthio anion CH2=CHS− can be observed as a result of the direct addition of an hydrosulfide ion to acetylene with a barrier having a height ≤123 kJ/mole. 2. One of the interme