How do you name the compound HIO4? - Answers
2024年5月28日 · HIO4 (periodic acid) is commonly used in organic synthesis to cleave vicinal diols to aldehydes and ketones, a process known as periodate cleavage. This reaction is …
What is the formula name for HIO4? - Answers
2024年5月22日 · HIO4 is an iodine oxoacid widely referred to as periodic acid (in Dutch: Periodsaeure, and Ueberiodsaeure) and hyperiodic acid (as HIO4). It is also referred to as …
What is the oxidation number of HIO4? - Answers
2024年6月1日 · HIO4(aq) stands for periodic acid, which is a strong oxidizing agent commonly used in organic chemistry for oxidation reactions. It is a colorless, crystalline solid when in …
Why glucose and other similar carbohydrates are oxidised fully by …
2019年12月20日 · $\ce{HIO4_{(aq)}}$ requires the vicinal diols to have syn configuration, as it forms a cyclic periodate ester. But glucose does not have syn configuration at C3 , and if you …
Acid strengths for HBrO4 vs HIO4, and HBr vs HI
2016年8月14日 · $\ce{HBrO4}$ and $\ce{HIO4}$ both have the acidic proton bound to oxygen: The H-O bond is approximately of equal strength in both acids and therefore you turn to …
Periodic cleavage of carbohydrates - Chemistry Stack Exchange
2015年4月30日 · Carbohydrate like glucose undergoes periodic cleavage by $\ce{HIO4}$ and forms respective products are five moles of formic acid and one mole of formaldehyde. Here is …
What are the uses of reagents HIO4 in organic synthesis?
2024年6月1日 · HIO4 (periodic acid) is commonly used in organic synthesis to cleave vicinal diols to aldehydes and ketones, a process known as periodate cleavage. This reaction is useful for …
organic chemistry - Oxidation of hydroxyl groups of glucose
2020年8月21日 · The presence of several pairs of vicinal diols such as those in glucose during oxidation with $\ce{HIO4}$ can lead to the formation of complex product mixtures: Accordingly, …
Standard Half-Cell Reduction Potential for Periodate to Iodine
I'm looking for standard half-cell reduction potential $\ce{IO4-}$/$\ce{I2}$ in acid medium. Unfortunately I was unable to find the value in all comprehensible reference books.
Effect of periodic acid on cyclohexane derivatives
Periodic acid (per-iodic acid, $\ce{HIO4}$ ) cleaves vicinal diols(to carbonyls) via a cyclic intermediate. Due to the cyclic intermediate, it needs a syn configuration for the $\ce{-OH}$ …