The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents because of the explosive tendencies of aromatic nitro compounds which increase in the presence of multiple nitro groups.
32.
The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents because of the explosive tendencies of aromatic nitro compounds which increase in the presence of multiple nitro groups.
33.
In Asimov's writings the endochronicity of thiotimoline is explained by the fact that in the thiotimoline molecule, there is at least one carbon atom such that, while two of the carbon's four chemical bonds lie in normal amino groups, and one sulfonic acid group, and possibly one nitro compound group as well.
34.
This includes the conversion of unreactive alkyl nitro compounds to their corresponding dianions which will react faster with carbonyl substrates, reactions can be accelerated using PAP as base, utilization of the reactivity of aldehydes with ?, ?-doubly deprotonated nitroalkanes to give nitronate alkoxides that yield mainly syn-nitro alcohols once protonated, and finally generation of nitronate anions in which one oxygenatom on the nitro group is silyl-protected to yield anti-?-nitro alcohols in the presence of a fluoride anion source when reacted with an aldehyde.
