November 01, 2024, 07:35:11 AM
Forum Rules: Read This Before Posting


Topic: IUPAC Names  (Read 9160 times)

0 Members and 1 Guest are viewing this topic.

Offline ritwik08

  • Regular Member
  • ***
  • Posts: 26
  • Mole Snacks: +0/-0
IUPAC Names
« on: October 07, 2008, 12:04:03 PM »
NC-CH2-CH2-COOH
Will the C of CN be counted in main chain????

Offline macman104

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 1644
  • Mole Snacks: +168/-26
  • Gender: Male
Re: IUPAC Names
« Reply #1 on: October 07, 2008, 12:24:07 PM »
No.  The CN group is a cyano group, and it is not counted as part of the parent chain.

Offline ritwik08

  • Regular Member
  • ***
  • Posts: 26
  • Mole Snacks: +0/-0
Re: IUPAC Names
« Reply #2 on: October 07, 2008, 01:05:20 PM »
No.  The CN group is a cyano group, and it is not counted as part of the parent chain.
Thats exactly what I thought. But my teacher has marked me wrong for not counting the carbon in CN. Can you supplement this argument with a reliable source please?

Offline macman104

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 1644
  • Mole Snacks: +168/-26
  • Gender: Male
Re: IUPAC Names
« Reply #3 on: October 07, 2008, 01:09:14 PM »
What did you put as your answer that was marked wrong?

Offline azmanam

  • Chemist
  • Sr. Member
  • *
  • Posts: 1416
  • Mole Snacks: +160/-24
  • Mediocrity is a handrail -Charles Louis d'Secondat
Re: IUPAC Names
« Reply #4 on: October 07, 2008, 01:13:22 PM »
I think it depends if the nitrile is the highest priority substituent or not.  If it is, the carbon is included in the backbone and it is named as a 1-nitrile.  If there is a higher priority substituent, the carbon is not included in the chain and the C-N triple bond is named as a cyano group.

In this example, I would say the acid is highest priority and the compound should be named 3-cyano-propanoic acid (ChemDraw agrees).

http://www.chem.ucalgary.ca/courses/351/orgnom/nitriles/nitriles-01.html
Knowing why you got a question wrong is better than knowing that you got a question right.

Offline ritwik08

  • Regular Member
  • ***
  • Posts: 26
  • Mole Snacks: +0/-0
Re: IUPAC Names
« Reply #5 on: October 07, 2008, 09:15:08 PM »
What did you put as your answer that was marked wrong?
I put:
3-cyano-propan-1-oic acid
but he says it should be
4-cyano-butan-1-oic acid

Offline macman104

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 1644
  • Mole Snacks: +168/-26
  • Gender: Male
Re: IUPAC Names
« Reply #6 on: October 08, 2008, 03:56:40 AM »
I disagree with your professor.

Go to this site:

http://www.lookchem.com/cas-160/16051-87-9.html

Give him the CAS number and tell him to double-check if he doesn't believe you.

Offline azmanam

  • Chemist
  • Sr. Member
  • *
  • Posts: 1416
  • Mole Snacks: +160/-24
  • Mediocrity is a handrail -Charles Louis d'Secondat
Re: IUPAC Names
« Reply #7 on: October 08, 2008, 08:11:32 AM »
fyi - While not technically incorrect, the -1- before the -oic acid is redundant.  Carboxylic acids, by definition, must be at the 1 position of the longest linear chain.

Even ChemSpider -- notorious for having every possible name of a compound (and some impossible names) -- says that compound is 3-cyanopropanoic acid only.

http://www.chemspider.com/Chemical-Structure.231083.html
Knowing why you got a question wrong is better than knowing that you got a question right.

Offline Borek

  • Mr. pH
  • Administrator
  • Deity Member
  • *
  • Posts: 27820
  • Mole Snacks: +1808/-412
  • Gender: Male
  • I am known to be occasionally wrong.
    • Chembuddy
Re: IUPAC Names
« Reply #8 on: October 08, 2008, 09:19:03 AM »
Carboxylic acids, by definition, must be at the 1 position of the longest linear chain.

What about...
ChemBuddy chemical calculators - stoichiometry, pH, concentration, buffer preparation, titrations.info

Offline azmanam

  • Chemist
  • Sr. Member
  • *
  • Posts: 1416
  • Mole Snacks: +160/-24
  • Mediocrity is a handrail -Charles Louis d'Secondat
Re: IUPAC Names
« Reply #9 on: October 08, 2008, 09:32:00 AM »
touche.  Gotta pull out the exceptions, don't you?  :)

So the acid defines the parent chain, and is by definition at position 1.  That might be a more precise way to say it.  Your example would be 2-ethylbutanoic acid.
Knowing why you got a question wrong is better than knowing that you got a question right.

Offline Borek

  • Mr. pH
  • Administrator
  • Deity Member
  • *
  • Posts: 27820
  • Mole Snacks: +1808/-412
  • Gender: Male
  • I am known to be occasionally wrong.
    • Chembuddy
Re: IUPAC Names
« Reply #10 on: October 08, 2008, 09:38:36 AM »
touche.  Gotta pull out the exceptions, don't you?  :)

That's the way my brain is wired. I don't even have to think about counterexamples, they just lie around :)
ChemBuddy chemical calculators - stoichiometry, pH, concentration, buffer preparation, titrations.info

Offline ritwik08

  • Regular Member
  • ***
  • Posts: 26
  • Mole Snacks: +0/-0
Re: IUPAC Names
« Reply #11 on: October 08, 2008, 09:44:17 AM »
Thanks guys for those proofs. Thanks once again. I will give him the CAS number, but there is little chance that he would pay heed to my argument.

Offline DrCMS

  • Chemist
  • Sr. Member
  • *
  • Posts: 1303
  • Mole Snacks: +211/-84
  • Gender: Male
Re: IUPAC Names
« Reply #12 on: October 09, 2008, 05:37:48 AM »
Your teacher is confused and wrong.

Heres why:

With only the CN group there the carbon of the CN is included in the longest chain name with the CN denoted as a nitrile.

NC-CH2-CH2-CH3  is butanenitrile

With the acid group as well the longest chain is named for the acid with the CN as a cyano group

NC-CH2-CH2-COOH  is 3-cyanopropanoic acid

See this for the IUPAC proof of this:

http://www.acdlabs.com/iupac/nomenclature/93/r93_557.htm

Sponsored Links