Chemistry, asked by nuraibrahim192, 8 months ago

how the aldehydes became carboxylic acids

Answers

Answered by Anonymous

The oxidation of aldehydes to carboxylic acids is a two-step procedure. In the first step, one mol of water is added in the presence of an acidic catalyst to generate a hydrate (geminal 1,1-diol). Subsequently, the hydrate is oxidized to the carboxylic acid formally eliminating water.

$<!DOCTYPE html><html lang="en"><head><title>Doraemon</title></head><body><div class="head"><div class="eye_white"><ul><li><div class="eye_black"></div></li><li><div class="eye_black"></div></li></ul></div><div class="white"><div class="line_left"></div><div class="line_right"></div><div class="nose"></div><div class="line_vertical"></div><div class="mouth"></div></div></div><style>.head{width:600px;height:600px;border-radius:100%;background:#3c9dca;border: black solid thick;}.white{width: 524px;height: 462px;border-radius: 100%;position: relative;top: 120px;left: 38px;background: #FFF;border: black solid thin;z-index: 0;}.eye_white {position: relative;top: 60px;left: 130px;z-index: 1;}.eye_white li{width: 125px;height: 152px;border-radius: 100%;background: #FFF;list-style:none;border: black solid thin;display:block;float:left;}.eye_black{width: 25px;height: 45px;border-radius: 100%;background: #000;list-style:none;top: 80px;position:relative;border: black solid thin;display:block;left: 10px;-webkit-animation:move 6s ease infinite;animation:move 6s ease infinite;}@-webkit-keyframes move {16%{top:95px;left:30px;}32%{top:100px;left:60px;}48%{top:80px;left:90px}64%{top:100px;left:60px}80%{top:95px;left:30px}}@keyframes move {16%{top:95px;left:30px;}32%{top:100px;left:60px;}48%{top:80px;left:90px}64%{top:100px;left:60px}80%{top:95px;left:30px}}.eye_black::before{content:'';width: 10px;height: 15px;border-radius: 100%;background: #fff;list-style: none;top: 16px;position: relative;display: block;left: 7px;}.line_left{width: 150px;height:2px;transform:rotate(20deg);top: 90px;left: 14px;position:relative;border-radius: 10%;background: #000;list-style: none;display: block;}.line_left::before{content:'';width: 150px;height:2px;top: 70px;transform:rotate(-20deg);position:relative;border-radius: 10%;background: #000;list-style: none;display: block;}.line_left::after{content:'';transform:rotate(-40deg);width: 150px;height:2px;top: 120px;left: 30px;position:relative;border-radius: 10%;background: #000;list-style: none;display: block;}.line_right{width: 150px;height:2px;transform:rotate(160deg);top: 90px;left: 370px;position:relative;border-radius: 10%;background: #000;list-style: none;display: block;}.line_right::before{content:'';width: 150px;height:2px;bottom: 100px;position:relative;transform:rotate(30deg);border-radius: 10%;background: #000;list-style: none;display: block;left:20px;}.line_right::after{content:'';width: 150px;height:2px;bottom: 50px;transform:rotate(10deg);left: 0px;position:relative;border-radius: 10%;background: #000;list-style: none;display: block;}.nose{width: 45px;height: 45px;border-radius: 100%;background: #b90319;list-style: none;top: 60px;position: relative;border: black solid thin;display: block;left: 236px;z-index:2;}.nose::after{content: '';width: 15px;height: 15px;border-radius: 100%;background: #FFF;list-style: none;top: 19px;position: relative;border: black solid thin;display: block;left: 9px;}.line_vertical{width: 2px;height: 310px;top: 40px;left: 258px;position: relative;border-radius: 10%;background: #000;z-index: 1;}.mouth{width: 400px;height: 400px;border-radius: 100%;top: -358px;left: 62px;position: relative;background: #000;z-index: -1;}.mouth::after{content: '';width: 402px;height: 401px;top: -4px;left: -1px;border-radius: 100%;position: relative;display: block;background: #FFF;}</style></body></html>$

Answered by ItsCrazyDaRk02

Answer:

The oxidation of aldehydes to carboxylic acids is a two-step procedure. In the first step, one mol of water is added in the presence of an acidic catalyst to generate a hydrate (geminal 1,1-diol).

Previous Question

Next Question