As a physical chemist it just pains me that the procedure is:
Step 1. Twist the poor molecule in to the highest possible energy conformation that it will probably never obtain at temperatures below its decomposition point. . . .
@rangek I tell students the Fischer and Haworth projections are meant (1) to unambiguously reflect the stereochemistry at each chiral center (2) to be convenient for early 20th-century letterpress print shops (3) not to be clear for undergraduate novices
I will never get used to chemfig, it is too much for me. I drew some natural compound in chemfig _by hand_ for my 12th project. Thankfully, I didnt go the organic route; I would have lost all my hair if I had to draw those mechanisms all in chemfig.
Vicomte Folmer af Helvede
in reply to James Endres Howell • • •James Endres Howell
in reply to Vicomte Folmer af Helvede • • •@folfdk Hope this is useful!
codeberg.org/jamesendreshowell…
chemfig-examples
Codeberg.orghajovonta
in reply to James Endres Howell • • •There is no code in the org 😀
@folfdk
James Endres Howell
in reply to hajovonta • • •@hajovonta @folfdk
codeberg.org/jamesendreshowell…
rangek
in reply to James Endres Howell • • •Ugh. Fischer projections. How they vex me.
But this is super cool.
James Endres Howell
in reply to rangek • • •Fischer Projection Mnemonic: the Prize Wheel on The Price is Right.
Vertical lines go back.
YOU'RE WELCOME #MCAT HUSTLERS
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rangek
in reply to James Endres Howell • • •😆
As a physical chemist it just pains me that the procedure is:
Step 1. Twist the poor molecule in to the highest possible energy conformation that it will probably never obtain at temperatures below its decomposition point.
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.
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rangek
in reply to rangek • • •Sensitive content
James Endres Howell
in reply to rangek • • •James Endres Howell
in reply to James Endres Howell • • •visuwesh
in reply to James Endres Howell • • •