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Chiral atom

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chiral atom is the one that has all R diferent. example, CR4 is chiral if R1,R2,R3,R4 r diferent. those atoms can be opticaly active... u must heard of D or L sugars... it has to do with chirality... :naughty:

 

An atom can be a chiral center if it has 4 different atoms/groups attached, such as an asymetrical carbon atom, but it is the molecule that would be chiral.

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Argh! Chemistry...I hated that class. It was fun...maybe if i actually paid attention in that class..o well

Welcome never the less. My name is Open Mind 5 and i will be about this site, if u need naything just call, and as everyone said, english is not a problem...i am sure their are brains here that can understand u!

 

Op5

 

-Prepare your mind to be opened!

Hu-HA-

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An atom can be a chiral center if it has 4 different atoms/groups attached, such as an asymetrical carbon atom, but it is the molecule that would be chiral.

u r right. i just didnt wanna to bother with chem-dictionary... by the way new chemist calls himself chiralAtom :naughty:

for me u r shinny big A of organic chemistry, stereochemistry well done !

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chiral atom is the one that has all R diferent. example, CR4 is chiral if R1,R2,R3,R4 r diferent. those atoms can be opticaly active... u must heard of D or L sugars... it has to do with chirality... :naughty:

 

That is sloppy at best and plain wrong at worst. An isolated chiral tetrahedral carbon atom can certainly have four different groups. It can also have four rigorously identical groups, be undistorted, and still be chiral if it has point group T (not T_d or T_h) symmetry. An example is the central carbon in [6.6]chiralane,

 

http://www.mazepath.com/uncleal/chiral2.gif

http://www.mazepath.com/uncleal/chiral3.gif

 

Where is the "chiral atom" in a helicene? In a binaphthyl? In a trans-cycloalkene?

 

Chirality is defined by symmetry - absence of an inversion point, mirror planes, and higher S_n axes of symmetry - not by substitution.

 

All isolated atoms are intrinsically homochiral via the Weak Interaction and neutral current (Z_0 exchange, nucleus to orbiting electrons). The effect is very weak even in the heaviest elements even with interaction strength scaling as (atomic weight)^4.

 

Mendeleev Commun. 13(3) 129 (2003)

http://socrates.berkeley.edu/~budker/PubList.html

Phys. Rev. Lett. 82(12) 2484 (1999)

Phys. Rev. Lett. 80(17) 3719 (1998)

Rep. Prog. Phys. 60(11) 1351 (1997)

Phys. Rev. A 52(3) 1895 (1995)

Am. J. Phys. 56 1086 (1988)

http://arXiv.org/abs/cond-mat/0207627

 

--

Uncle Al

http://www.mazepath.com/uncleal/

(Toxic URL! Unsafe for children and most mammals)

http://www.mazepath.com/uncleal/qz.pdf

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Ahhh...the wonders of stereochemistry...

 

While the mechanics of stereo chemistry were way too fun in organic (I think I would rather have pins shoved under my nails than have to go to another organic lab and watch something reflux in a fractional distilation tube for an hour or so again) the implications of it in the biological realm are quite fascinating. The abiolity of our body to only produce certain molecules with a specific chirality is amazing (We can barely do it iunder some circumstances in the lab). Along with that is the chiral specific interactions in the body. Coooll.... :naughty:

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Organic chemistry is life; everything else is waiting. Explanations of biological homochirality's origin are poor at best (read: pathetic),

 

Angew. Chem. Int. Ed. 41(24) 4619 (2002)

Angew. Chem. Int. Ed. 41(7) 1139 (2002)

Angew. Chem. Int. Ed. 39(22) 4033 (2000)

Chem. Phys. Chem. 2(7) 409 (2001)

Phys. Rev. Lett. 84(17) 3811 (2000)

 

Quantitative geometric chirality is rigorously defned by mathematican Michel Petitjean, including its calculation in QCM software,

 

Petitjean, Michel, J. Math. Phys. 43(8) 4147 (2002)

http://petitjeanmichel.free.fr/itoweb.petitjean.html

http://petitjeanmichel.free.fr/itoweb.petitjean.freeware.html#QCM

 

It's a truly nasty field to study as pure math,

 

http://www.mdpi.net/entropy/papers/e5030271.pdf

Review of quantitative geometric chirality

 

As long as you are in homogeneous isotropic solution, an organiker's view is good enough for an organiker(e.g., ORD spectroscopy) even though it has little rigor and is seriously wrong at its edges,

 

J. Mol. Phys. 43(6) 1395 (1981)

J. Appl. Cryst. 19 108 (1986)

J. Chem. Phys. 65(4) 1522 (1976)

 

Angew. Chem. Int. Ed. 38 3418 (1999)

Chem. Rev. 98(7) 2391 (1998)

J. Am. Chem. Soc. 108 5539 (1986)

Nature 405(6789) 932 (2000)

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organic chemistry is vocabulary to biocemistry... IT IS WHAT WE R!!! ORGANIC

 

Lexan polycarbonate and a ton of other compounds, including dozens of amino acids, are organic, but they're not (naturally) found in living organisms.

 

Biochemistry ... IT IS WHAT WE ARE!!!!

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amono acids not found in organisms???? do u know what u wrote?...

and hello! u need to be the best organicher if u tend to become biochemist, scientific one, more chem less biology with is describleble science, not exact as chemsitry, math or phisics

ps if u dont know other living forms it doesnt mean that they dont exsist :hyper:

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