Reactions of Amines

An organic compound derived by replacing one or more of the hydrogen atoms of ammonia with alkyl or aromatic groups, as in RNH2, R2NH, and R3N.

[@deegegaming7911]

This is a golden 6 minutes of chemistry teaching, just what i needed thsnks

[@আবুউবায়দা]

Thank you sir..I am from Bangladesh.. First time i enjoyed your lecture.. I will follow you.

[@marthapepin9355]

Thank you for your explanation this was extremely helpful. Tomorrow I have a organic exam and was not sure of anime and amides. But you helped me get a little closer.

[@edtruong1676]

“anime”

[@thandiweluluphiri5]

Thank you sir so much love from me.

[@worldchange3009]

Hi

[@zaharadeenmukhtar7137]

its my pleasure to express you thank because,I found it easy to understand the basic of chemistry

[@maritzamasgo182]

Thank you very much!!!! It helped a great deal, just when I needed.

[@worldchange3009]

Hi mam

[@JAD705-JA]

The best lecturer in the world!!!!!!!

[@സത്യമേവജയാതെ-ശ3വ]

Thank you sir l am from India ,, great class so helpfull🙏🏻😊

[@niclettekembi7223]

Great video! I'm a little confuse with the rxns #3. I think, the reaction will yield H2o as well.

[@camilaramirez6705]

Thank you, great video.

[@worldchange3009]

I need your email or WhatsApp no

[@johnblacksuperchemist2556]

QUESTION..........Why does NH4Cl and formaldehyde make methylamine and not an imine????????? NH4Cl in water (from the formalin) will have NH3 in it. So it should do a reductive amination reaction forming an imine. But for some reason it forms an amine. If it does form an imine intermediate then how does that turn in to an amine. I mean if you protonate once to get an iminium ion then you can not protonate a second time to get rid of the double bond form the imine. There are no hydride anions to attack the imine. So how does the imine get reduced to an amine???????????

[@call2God]

عمي بشدة شرحك يخبل استمر بس ديربالك لتطلع ويصير بيك كورونا خرب خلي يموت الصدر ولا انت يربك

[@mo7amed7amedo3afify4]

Carlo Ancelotti 😂😂

[@nikkier2409]

Is water (H2O) also a product in # 3 reaction?

[@christineabdulkarim4456]

This is a really good tutorial

[@worldchange3009]

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[@worldchange3009]

I need your WhatsApp number or email address

[@gamexpose6301]

To get the amine back by adding water, shouldn't you get NaCl, the anime AND water because of the H+ and the OH-??

[@osmanahmed7810]

yes you should because if you react anything with a hydroxide, such as NaOH, then one of the products is going to be water

[@gavish123]

Where is oxidation of amines ?????

[@anandganvir7156]

Primary and secondary amines give carbonyl compounds

[@thalapathysakthidharan391]

@@anandganvir7156 tertiary gives nitro componds

[@sagarmagarde7124]

clorine stable hone ke bad bhi bond kaise bna rha ??

[@madhudeogharia5607]

In logo ko hindi nahi aati.🙈
Waise chlorine dipole mein change ho jata hai .isiliye wo react karta hai.
And usko ek electron bhi chhahiye.

[@letscollect7875]

Above you write reactions of amines but here reactions of amide😕

[@vishnusanthosh7599]

they have it very easy

[@anthenriqe909]

#2 is methamphetamines

[@Kayweezyfbabyy]

Thank you everyone right this in line angle and I hate it so thanks

[@Icecube1256]

Dont wanna hear about your horoscopes.