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関連する概念動画

Acids, Bases and Neutralization Reactions03:26

Acids, Bases and Neutralization Reactions

An acid-base reaction is one in which a hydrogen ion, H+, is transferred from one chemical species to another. Such reactions are of central importance to numerous natural and technological processes, ranging from the chemical transformations within cells or lakes and oceans to the industrial-scale production of fertilizers, pharmaceuticals, and other substances essential to the society.
Preparation of Acid Anhydrides01:07

Preparation of Acid Anhydrides

One of the methods for preparing symmetrical or unsymmetrical acid anhydrides involves the treatment of acid chlorides with the sodium salt of carboxylic acids. The reaction proceeds via a nucleophilic acyl substitution.
The carboxylate ion acts as a nucleophile that attacks the carbonyl carbon of the acid chloride to form a tetrahedral intermediate. Subsequently, the re-formation of the carbonyl group with the loss of the chloride ion as a leaving group leads to the formation of an acid...
Diazonium Group Substitution: –OH and –H01:19

Diazonium Group Substitution: –OH and –H

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.
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism01:37

1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism

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.
Acids, Bases and Neutralization Reactions01:27

Acids, Bases and Neutralization Reactions

Acids and bases play several important roles in biology. The pH of a biological system can significantly impact the function of biological molecules, including enzymes, proteins, and nucleic acids. For example, enzymes have optimal pH ranges for their activity, and changes in pH can denature or alter their structure, affecting their function. Acids and bases also play a crucial role in cellular signaling and communication. The pH of the extracellular fluid around cells can influence the...
Production of Organic Acids01:25

Production of Organic Acids

Lactic acid, an important organic acid extensively applied in food, pharmaceutical, and biodegradable polymer industries, is primarily produced via microbial fermentation. This method is favored over chemical synthesis due to its environmental sustainability and capacity for enantiomerically pure product formation. Among various microbial processes, the fermentation of starch-based substrates stands out due to the abundance and renewability of raw materials like corn and potatoes.Hydrolysis of...

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関連する実験動画

Updated: Jul 13, 2026

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
11:14

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent

Published on: February 21, 2017

室温でピリジンボランを用いた水酸化処理.

Julia M Clay1, Edwin Vedejs

  • 1Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.

Journal of the American Chemical Society
|April 21, 2005
PubMed
まとめ

新しいピリジンボラン複合体は,アルケンを室温で水酸化するために活性化します. この方法は,選択的なモノアダクト形成と,有用なカリウムアルキルトリフルオロボラート塩への簡単な変換を提供します.

科学分野:

  • 有機化学 オーガニック・ケミストリー
  • オルガノボロン化学 オルガノボロン化学

背景:

  • ピリジンボラン (Py.BH3) は,有機合成に使用される反応剤である.
  • 水酸化はアルケンの機能化のための重要な反応である.

研究 の 目的:

  • 効率的な水酸化のための活性化ピリジンボラン複合体を開発する.
  • この新しい水酸化反応のメカニズムを調査するために.
  • ハイドロブラーション製品からアルキルトリフローロボラート塩を合成する.

主な方法:

  • ピリジンボランをヨウ素,ブロミン,または強い酸で処理して,Py.BH2X複合体を形成する.
  • Py.BH2X複合体の反応とアルケンの反応.
  • メタノリックKHF2.2を用いて,ヒドロボレーション製品のカリウムアルキルトリフローロボラート塩への変換.

主要な成果:

  • 活性化されたPy.BH2X複合体は,室温でアルケンを効果的に水酸化する.
  • 証拠によると,異例の水力採掘機構があり,集団の移動を伴う.
  • Py.BH2Iは,THF.BH3.3とは異なり,選択的にモノアダクトを生成します.
  • 原材料は容易にアルキルトリフローロボラート塩のカリウムに変換されます.

さらに関連する動画

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
08:15

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts

Published on: February 7, 2017

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
08:05

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O

Published on: October 7, 2020

関連する実験動画

Last Updated: Jul 13, 2026

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
11:14

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent

Published on: February 21, 2017

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
08:15

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts

Published on: February 7, 2017

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
08:05

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O

Published on: October 7, 2020

結論:

  • 活性化ピリジンボラン複合体は,アルケンの水酸化のための多用途で選択的な方法を提供します.
  • この反応は,ユニークなメカニズムによって進行します.
  • その結果生成されるトリフローロボラート塩は,価値ある合成中間物質である.