Azo coupling in aromatic amines
I thought of two products that can be formed in azo coupling of aniline but can't decide which one is major so basically I need an answer to which product is major and why ? Thanks in advance😊
organic-chemistry reaction-mechanism
add a comment |
I thought of two products that can be formed in azo coupling of aniline but can't decide which one is major so basically I need an answer to which product is major and why ? Thanks in advance😊
organic-chemistry reaction-mechanism
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago
add a comment |
I thought of two products that can be formed in azo coupling of aniline but can't decide which one is major so basically I need an answer to which product is major and why ? Thanks in advance😊
organic-chemistry reaction-mechanism
I thought of two products that can be formed in azo coupling of aniline but can't decide which one is major so basically I need an answer to which product is major and why ? Thanks in advance😊
organic-chemistry reaction-mechanism
organic-chemistry reaction-mechanism
asked 2 hours ago
Aditya Garg
1293
1293
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago
add a comment |
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago
add a comment |
1 Answer
1
active
oldest
votes
This is a really interesting question and the answer is that the reaction of benzenediazonium chloride with aniline is a bit different to most of the reactions of benzenediazonium salts in that the initial product is the top compound diazoaminobenzene. It is possible to run the reaction to isolate diazoaminobenzene prep here. These diazoaminobenzene compounds are unstable with respect to reversion to a diazonium salt + nucleophile, and so many references suggest that the bottom product (4-aminoazobenzene) is directly produced. The procedure for the transformation of the diazaminobenzene to 4-aminoazobenzene is by heating to 50C with aniline prep here.
add a comment |
Your Answer
StackExchange.ifUsing("editor", function () {
return StackExchange.using("mathjaxEditing", function () {
StackExchange.MarkdownEditor.creationCallbacks.add(function (editor, postfix) {
StackExchange.mathjaxEditing.prepareWmdForMathJax(editor, postfix, [["$", "$"], ["\\(","\\)"]]);
});
});
}, "mathjax-editing");
StackExchange.ready(function() {
var channelOptions = {
tags: "".split(" "),
id: "431"
};
initTagRenderer("".split(" "), "".split(" "), channelOptions);
StackExchange.using("externalEditor", function() {
// Have to fire editor after snippets, if snippets enabled
if (StackExchange.settings.snippets.snippetsEnabled) {
StackExchange.using("snippets", function() {
createEditor();
});
}
else {
createEditor();
}
});
function createEditor() {
StackExchange.prepareEditor({
heartbeatType: 'answer',
autoActivateHeartbeat: false,
convertImagesToLinks: false,
noModals: true,
showLowRepImageUploadWarning: true,
reputationToPostImages: null,
bindNavPrevention: true,
postfix: "",
imageUploader: {
brandingHtml: "Powered by u003ca class="icon-imgur-white" href="https://imgur.com/"u003eu003c/au003e",
contentPolicyHtml: "User contributions licensed under u003ca href="https://creativecommons.org/licenses/by-sa/3.0/"u003ecc by-sa 3.0 with attribution requiredu003c/au003e u003ca href="https://stackoverflow.com/legal/content-policy"u003e(content policy)u003c/au003e",
allowUrls: true
},
onDemand: true,
discardSelector: ".discard-answer"
,immediatelyShowMarkdownHelp:true
});
}
});
Sign up or log in
StackExchange.ready(function () {
StackExchange.helpers.onClickDraftSave('#login-link');
});
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
StackExchange.ready(
function () {
StackExchange.openid.initPostLogin('.new-post-login', 'https%3a%2f%2fchemistry.stackexchange.com%2fquestions%2f107344%2fazo-coupling-in-aromatic-amines%23new-answer', 'question_page');
}
);
Post as a guest
Required, but never shown
1 Answer
1
active
oldest
votes
1 Answer
1
active
oldest
votes
active
oldest
votes
active
oldest
votes
This is a really interesting question and the answer is that the reaction of benzenediazonium chloride with aniline is a bit different to most of the reactions of benzenediazonium salts in that the initial product is the top compound diazoaminobenzene. It is possible to run the reaction to isolate diazoaminobenzene prep here. These diazoaminobenzene compounds are unstable with respect to reversion to a diazonium salt + nucleophile, and so many references suggest that the bottom product (4-aminoazobenzene) is directly produced. The procedure for the transformation of the diazaminobenzene to 4-aminoazobenzene is by heating to 50C with aniline prep here.
add a comment |
This is a really interesting question and the answer is that the reaction of benzenediazonium chloride with aniline is a bit different to most of the reactions of benzenediazonium salts in that the initial product is the top compound diazoaminobenzene. It is possible to run the reaction to isolate diazoaminobenzene prep here. These diazoaminobenzene compounds are unstable with respect to reversion to a diazonium salt + nucleophile, and so many references suggest that the bottom product (4-aminoazobenzene) is directly produced. The procedure for the transformation of the diazaminobenzene to 4-aminoazobenzene is by heating to 50C with aniline prep here.
add a comment |
This is a really interesting question and the answer is that the reaction of benzenediazonium chloride with aniline is a bit different to most of the reactions of benzenediazonium salts in that the initial product is the top compound diazoaminobenzene. It is possible to run the reaction to isolate diazoaminobenzene prep here. These diazoaminobenzene compounds are unstable with respect to reversion to a diazonium salt + nucleophile, and so many references suggest that the bottom product (4-aminoazobenzene) is directly produced. The procedure for the transformation of the diazaminobenzene to 4-aminoazobenzene is by heating to 50C with aniline prep here.
This is a really interesting question and the answer is that the reaction of benzenediazonium chloride with aniline is a bit different to most of the reactions of benzenediazonium salts in that the initial product is the top compound diazoaminobenzene. It is possible to run the reaction to isolate diazoaminobenzene prep here. These diazoaminobenzene compounds are unstable with respect to reversion to a diazonium salt + nucleophile, and so many references suggest that the bottom product (4-aminoazobenzene) is directly produced. The procedure for the transformation of the diazaminobenzene to 4-aminoazobenzene is by heating to 50C with aniline prep here.
edited 47 mins ago
answered 1 hour ago
Waylander
5,79711021
5,79711021
add a comment |
add a comment |
Thanks for contributing an answer to Chemistry Stack Exchange!
- Please be sure to answer the question. Provide details and share your research!
But avoid …
- Asking for help, clarification, or responding to other answers.
- Making statements based on opinion; back them up with references or personal experience.
Use MathJax to format equations. MathJax reference.
To learn more, see our tips on writing great answers.
Some of your past answers have not been well-received, and you're in danger of being blocked from answering.
Please pay close attention to the following guidance:
- Please be sure to answer the question. Provide details and share your research!
But avoid …
- Asking for help, clarification, or responding to other answers.
- Making statements based on opinion; back them up with references or personal experience.
To learn more, see our tips on writing great answers.
Sign up or log in
StackExchange.ready(function () {
StackExchange.helpers.onClickDraftSave('#login-link');
});
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
StackExchange.ready(
function () {
StackExchange.openid.initPostLogin('.new-post-login', 'https%3a%2f%2fchemistry.stackexchange.com%2fquestions%2f107344%2fazo-coupling-in-aromatic-amines%23new-answer', 'question_page');
}
);
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function () {
StackExchange.helpers.onClickDraftSave('#login-link');
});
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function () {
StackExchange.helpers.onClickDraftSave('#login-link');
});
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function () {
StackExchange.helpers.onClickDraftSave('#login-link');
});
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Are you aware of the mechanism of the diazo coupling reaction?
– YUSUF HASAN
2 hours ago
Anyhow... Have a look at this
– YUSUF HASAN
1 hour ago
Can't realise how it helps??
– Aditya Garg
1 hour ago