Naming Amines - IUPAC Nomenclature & Common Names

[@TheOrganicChemistryTutor]

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sorry but how does he count the no of carbons, sometimes he count it from the back sometimes from the front, so how do you know if youre supposed to start counting from the back or front

[@user9371]

@@kingsleyc.649you start counting from the end of the chain that is closest to the nitrogen atom

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[@alsinbad3772]

IUPAC naming practice starts at 5:38 for those who needs it :)

[@wonghokyin8453]

and also the 'n' prefix he said after 5:38 is not IUPAC name. It just a common name......

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Translate them to portuguese.

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[@ishwar7856]

Just an information Its better to go with pentan-2-amine instead of 2pentanamine. It is accounted by the convention we followed ie alkan-1-amine.

[@Ntwenhle24]

Hey , so what happens if (please check on @11:00). If I follow what you're saying is methyl attached to octan-3-amine or do i add a dash after methyl?

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[@adriyaevans]

Nomenclature can get surprisingly overwhelming if you don’t know the basics. You make it so much easier to understand than my cramped textbook T-T

[@FaceByLilly_MUA]

Thank you, I'm not sure if I just skipped over it but I was trying to find examples of the IUPAC and common names too..

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[@pichuflash2769]

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[@Sussy.baka.]

6:57 Isn't it supposed to be named as butan-2-amine?

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[@fredericgilbert6742]

bro your a g didn't understand the N at the beginning of the name at all. Thanks so much

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[@jansentanu2637]

Great video..! But I suggest to also include the new nomenclature.

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[@indiecappuccino]

1:56 why isnt this methyl benenyl amine?

[@paysonkeown2960]

There isn’t a methyl group. The CH2 is already accounted for in the benzyl part of the name

[@indiecappuccino]

@@paysonkeown2960 ohh got it now.. thank you so much!

[@gauravGupta-bk2sw]

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[@andrewjustin256]

6:20 Could someone tell me why we are nomenclating it propanamine and not propylamine like the previous examples, please?

[@americanooo06]

propanamine is the iupac name and propylamine is the common name

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[@tsakanir363]

very helpful thank u 👏

[@charudharshini149]

At 11:50 N is bonded only 2 groups instead of 3

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[@oshaunaewilliams4173]

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[@leahgreene5880]

The IUPAC naming section uses the outdated system. You say, for example, 2-hexanamine when it should be hexan-2-amine. They're both technically correct, but the latter is prefered and depending on how picky they are, some professors may mark the first as wrong.

[@soumya534]

Yup...bt that can be neglected

[@liswanimuyatwa5421]

Yeah I thought so as well I think it's mostly Americans that use the first one

[@raanoooshh9296]

Thanks for implying that. I've noticed that my professor usually writes hexan-3-ol for example, instead of 3-hexanol. I study in Sweden btw.

[@jimhalpert9803]

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[@parthsinghal3733]

Extremely helpful!!

[@Andrew-kh7rz]

17:22 shoudn't be named N-methyl first instead of 3-ethyl because N takes priority?

[@falahmed6795]

E takes priority N,di,.... we don't count them when using alphabetical order..

[@Youngballer739]

I was wondering for questions like diethyl methylamine, we are not specifying where the 2 ethyl groups are located. Won't this affect polarity? For instance, at 4:30 the ethyl groups are on the left and middle, but what would happen if they were instead on the left and right with the methyl in the middle?

[@maximilianburger1636]

In this case not. First, its just the common name, there you don`t care about details like this. And second you would be right, if the N has 3 different substituents. But in this case, there are 2 ethyl-groups, that means the atom isn´t chiral so you can spin this whole molecule that the ethyl-groups are "inline" (not really inline because it has kind of a tetraedric structure but I hope you get my point)

[@jigishakashyap2700]

Thank you 👍🏻

[@painkiller8324]

Thank you 🦋😊

[@andrewjustin256]

1:44 Why is it cyclohexylamine and not cyclohexanamine?

[@kafhongchan8295]

Hi why the example for 5:14, we dont have to put N in front ya?

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[@Lulubluee19]

Thanks ❤

[@ImEatingCookies]

what about a carbon chain with NH? How would you go about naming that?

[@vjvjjvjv5729]

I think at 11:33 the nitrogen atom (N) must contain one hydrogen attached to it :).

[@sethdones3887]

or could be called 4-bromo-N-methylHexenamine

[@clips9675]

Can CH3NH2 be called 'methanamine'? I know it has a methyl group but according to my study book which has the IUPAC prefixes, doesn't 1 carbon indicate the 'meth-' preffix? So therefore, is it not 'methanamine'?

[@marif4654]

Methylamine

[@Bryan-zs4mz]

It can be called both, but more often is seen as methylamine

[@sajeenajunaid7652]

Cool! 😍👌👌 Thanks alot!

[@katiebellebaker9436]

Why does nitrogen have priority over Br in the example at 12:22? Bromine has a higher atomic number, so I'm a bit confused. If anyone could explain, I would be eternally grateful :)

[@paysonkeown2960]

By IUPAC naming rules, amines have a higher priority than halogens.

[@zainabadnan3647]

Thanks bro

[@soumya534]

In 12:14 u numbered the chain frm the middle??....if not then have u started numbering rom amine group??

[@rwayle]

He numbered from the N and went left, that chain is the parent carbon chain of that molecule.

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[@MansurMehdiyev-cx1uv]

thank you sir

[@greekfire7980]

5:02 Why isn't this " N-ethyl-N-methylpropanamine" ? According to 9:10 you name these amines like that^. Please answer, i don't get it...thank you in advance and thank you for the video.

[@Jojo-kl6tx]

I'm not sure, but I think the N is just used in IUPAC nomenclature. In trivial nomencmature you just name the substituents.

[@akshaykishoredesai2017]

@@Jojo-kl6txthis is common name nomenclature not IUPAC

[@shilpawaghe1989]

I Think when there are two methyl or any other 2 alkyl groups attached to amine we start naming it as N,N dimethylamine .....right?

[@raanoooshh9296]

Correct.

[@fatematuzzuhra6591]

Can't they be named as aminopropane, aminobutane etc.. instead of propylamine or butylamine?

[@ims1039]

Amatullah Maryam the amino group takes priority over the alkane

[@moshibudikgaogelo9383]

thank you so much

[@davincicode1918]

Thanks

[@sanjaidevil6440]

Arent they cyclohexanamine instead of hexyl /ethyl it should be hexane,ethan etc amine the are alkanamines not alkylamines if im correct?

[@vineetkumarchoudhary20]

Great sirrr

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Thank you 😊😍

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Thank u 🙏

[@bionic123]

Very useful

[@bennettegaper4344]

Thank you

[@zmkanzmkan4593]

Thank you man, really useful!

[@esraaatallah9914]

What is priority mean ?are mean the more powerful functional group?

[@beeliciouskitchen1920]

How do we know or master functional groups that has more priority

[@zoldyck2907]

kaway kaway sa mga taga bsu

[@ishwar7856]

Thanku verry much

[@ynady6110]

Im confused. Why do other referenced use heptanamine instead of heptylamine? Which follows the latest iupac nenclature?

[@oliviamulock413]

7:01 I thought that if the amino group was a side chain the name of the compound would have to start with amino rather than ending with amine

[@rwayle]

That's not a side chain though

[@rileymistycloe]

You say amino instead of ending with amine when another group has higher priority like if there was also an alcohol or carboxylate acid then you would consider the amine a substituent and call it an amino :)

[@mrzz1999]

Thanks alot