![Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry](https://cdn.masterorganicchemistry.com/wp-content/uploads/2019/12/1-tscl-and-mscl-toluenesulfonyl-chloride-and-mesyl-chloride-convert-alcohols-to-good-leaving-groups.gif)
Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry
![A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator - ScienceDirect A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403919308470-gr2.jpg)
A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator - ScienceDirect
![N-Sulfonylation of amines, imides, amides and anilides using p-TsCl in presence of atomized sodium in EtOH–THF under sonic condition - ScienceDirect N-Sulfonylation of amines, imides, amides and anilides using p-TsCl in presence of atomized sodium in EtOH–THF under sonic condition - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1350417715000322-fx1.jpg)
N-Sulfonylation of amines, imides, amides and anilides using p-TsCl in presence of atomized sodium in EtOH–THF under sonic condition - ScienceDirect
![What is the mechanism for the following alcohol with p-TsCl/pyridine followed by addition of a strong base | Study.com What is the mechanism for the following alcohol with p-TsCl/pyridine followed by addition of a strong base | Study.com](https://study.com/cimages/multimages/16/screen_shot_2020-06-09_at_9.45.12_am4867534232355080426.png)
What is the mechanism for the following alcohol with p-TsCl/pyridine followed by addition of a strong base | Study.com
![Reagents and conditions: (i) tosyl chloride (TsCl)/ pyridine, 60%, (ii)... | Download Scientific Diagram Reagents and conditions: (i) tosyl chloride (TsCl)/ pyridine, 60%, (ii)... | Download Scientific Diagram](https://www.researchgate.net/profile/Kartik-Soni/publication/236641067/figure/fig1/AS:375783953584128@1466605284125/Reagents-and-conditions-i-tosyl-chloride-TsCl-pyridine-60-ii-ethyl.png)
Reagents and conditions: (i) tosyl chloride (TsCl)/ pyridine, 60%, (ii)... | Download Scientific Diagram
![Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry](https://cdn.masterorganicchemistry.com/wp-content/uploads/2019/12/2-conversion-of-alcohol-to-ots-using-tscl.gif)
Reagent Friday: TsCl (p-toluenesulfonyl chloride) and MsCl (methanesulfonyl chloride) – Master Organic Chemistry
![Draw the structure of the product that is formed when the compound shown below is treated with the following reagents: 1) TsCI, pyridine; 2) NaBr. Show the appropriate stereochemistry. | Study.com Draw the structure of the product that is formed when the compound shown below is treated with the following reagents: 1) TsCI, pyridine; 2) NaBr. Show the appropriate stereochemistry. | Study.com](https://study.com/cimages/multimages/16/screen_shot_2020-02-01_at_12.01.21_pm5143522515790784054.png)
Draw the structure of the product that is formed when the compound shown below is treated with the following reagents: 1) TsCI, pyridine; 2) NaBr. Show the appropriate stereochemistry. | Study.com
![A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator - ScienceDirect A simple synthesis of ketone from carboxylic acid using tosyl chloride as an activator - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403919308470-ga1.jpg)