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Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

4.7K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
4.7K
Electrophilic Aromatic Substitution: Sulfonation of Benzene01:22

Electrophilic Aromatic Substitution: Sulfonation of Benzene

5.9K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
5.9K
Phase I Reactions: Reductive Reactions01:27

Phase I Reactions: Reductive Reactions

186
Phase I biotransformation reductive reactions are chemical processes that modify drugs by introducing or revealing polar functional groups via reduction. Enzymes called reductases catalyze these reactions, playing a pivotal role in drug metabolism by transforming lipophilic drugs into more polar, water-soluble metabolites for easy excretion. An essential type of reductive reaction is the carbonyl group reduction, where aldehydes and ketones are reduced to alcohols. An example is the...
186
Preparation and Reactions of Thiols02:33

Preparation and Reactions of Thiols

6.1K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
6.1K
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism01:18

Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

2.2K
Birch reduction uses solvated electrons as reducing agents. The reaction converts benzene to 1,4-cyclohexadiene. The reaction proceeds by the transfer of a single electron to the ring to form a benzene radical anion. This anion is highly basic—it abstracts a proton from the alcohol to form a cyclohexadienyl radical. Another single electron transfer gives the cyclohexadienyl anion. A proton transfer from the alcohol forms 1,4-cyclohexadiene. Since this reduction occurs via radical anion...
2.2K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.0K

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相关实验视频

Updated: Jun 15, 2025

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
09:16

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene

Published on: May 20, 2019

7.6K

硫重组:一种直接的方法.

R Koots1, G Brown1, J Pérez-Ríos1

  • 1Department of Physics and Astronomy, Stony Brook University, Stony Brook, New York 11790, USA.

The Journal of chemical physics
|August 27, 2024
PubMed
概括
此摘要是机器生成的。

这项研究使用经典轨迹模拟了硫重组反应 (S + S + M → S2 + M). 结果与实验数据非常一致,并突出了SAR反应通道的影响.

更多相关视频

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
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Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

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Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS
09:31

Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS

Published on: August 31, 2017

7.6K

相关实验视频

Last Updated: Jun 15, 2025

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
09:16

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene

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Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
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Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

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Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS
09:31

Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS

Published on: August 31, 2017

7.6K

科学领域:

  • 化学动力学 化学动力学
  • 大气化学 大气化学
  • 计算化学的计算化学

背景情况:

  • 硫的重组对于理解大气中的硫化学是至关重要的.
  • 之前的模型缺乏详细的三体重组数据.
  • 有实验数据,但需要理论验证.

研究的目的:

  • 为硫反应提供直接的三体重组方法.
  • 要计算S + S + M → S2 + M. 的比率.
  • 为了研究不同第三体 (M) 对反应速率的影响.

主要方法:

  • 超球坐标中的经典轨迹方法.
  • 模拟硫重组与 (Ar) 作为第三体.
  • 与298K的实验测量结果进行比较.

主要成果:

  • 计算显示出与M = Ar的实验数据的良好一致.
  • 二氧化硫 (S2) 生产受到SAR反应通道的显著影响.
  • 使用硫化 (H2S) 作为第三体,重组率没有显著变化.

结论:

  • 经典轨迹方法准确地模拟了硫的重组.
  • 在S2形成过程中,SAR通道起着关键作用.
  • 第三体的选择 (Ar与H2S) 对研究温度范围内的重组率的影响有限.