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The redox reaction behind iodometric titration: iodine and sodium thiosulfate. • Sodium thiosulfate, Na₂S₂O₃, is a white crystalline solid that dissolves in water, giving us the thiosulfate anion, S₂O₃²⁻, which is acting as a reducing agent in this demonstration. • Elemental iodine is slightly soluble in water, so in this brown coloured lugol’s iodine we have here it is mixed with potassium iodide to increase solubility via the formation of triiodide ions, I₃⁻ in the following exergonic equilibr

The redox reaction behind iodometric titration: iodine and so…

572 viewsJun 3, 2023

FacebookThe Cockney Chemist

SOLVED:Answer true or false. (a) The functional group of a thiol is the -SH (sulfhydryl) group. (b) The parent name of a thiol is the name of the longest carbon chain that contains the - SH group. (c) The S-H bond is nonpolar covalent. (d) The acidity of ethanethiol is comparable to that of phenol. (e) Both phenols and thiols are classified as weak acids. (f) The most common biological reaction of thiols is their oxidation to disulfides. (g) The functional group of a disulfide is the -S-S- group

SOLVED:Answer true or false. (a) The functional group of a thiol is t…

SOLVED:Thiols can be prepared from the reaction of thiourea with an alkyl halide, followed by hydroxide-ion-promoted hydrolysis. a. Propose a mechanism for the reaction. b. What thiol would be formed if the alkyl halide employed were pentyl bromide?

SOLVED:Thiols can be prepared from the reaction of thiourea with …

Thiols can be prepared from the reaction of thiourea with an alkyl halide, followed by hydroxide-ion-promoted hydrolysis. a. Propose a mechanism for the reaction. b. What thiol will be formed if the alkyl halide employed is pentyl bromide? | Numerade

Thiols can be prepared from the reaction of thiourea with an alkyl …

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