JoVE - Journal of Visualized Experiments
JoVE Visualize
Contact Us
这页已由机器翻译。其他页面可能仍然显示为英文。 View in English

用第15组集群进行催化氧化降解

  • 0Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford OX1 3QR, U.K.
Journal of the American Chemical Society +

|

2025年八月6日

在PubMed上查看摘要

概括

此摘要是机器生成的。

相关概念视频

<em data-lazy-src=

5.8K

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...

Catalysis 02:50

27.6K

The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.

The illustrated image represents the reaction diagrams for an endothermic chemical process progressing in the absence (red curve) and presence (blue curve) of a catalyst.

Diazonium Group Substitution: –OH and –H 01:19

2.9K

Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.

Figure 1.
A primary arylamine attacks the nitrosonium ion to form an...

Noble Gases 02:54

18.0K


The elements in group 18 are noble gases (helium, neon, argon, krypton, xenon, and radon). They earned the name “noble” because they were assumed to be nonreactive since they have filled valence shells. In 1962, Dr. Neil Bartlett at the University of British Columbia proved this assumption to be false.

These elements are present in the atmosphere in small amounts. Some natural gas contains 1–2% helium by mass. Helium is isolated from natural gas by liquefying the condensable...

2° Amines to <em data-lazy-src=

4.6K

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.

Figure 1. The nitration reaction of secondary amines
The...

1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO<sub data-lazy-src=

4.0K

Nitrous acid is a relatively weak and unstable acid prepared in situ by the reaction of sodium nitrite and cold, dilute hydrochloric acid. In an acidic solution, the nitrous acid undergoes protonation when it loses water to form a nitrosonium ion—an electrophile. Nitrous acid reacts with primary amines to give diazonium salts. The reaction is called diazotization of primary amines.

Figure 1. The mechanism of the diazotization reaction of primary amines.
As illustrated in Figure 1, in the...