Conformations Memes

Posts tagged with Conformations

Why Is The Height Of Ethane Rotation Barrier Nerfed?

Why Is The Height Of Ethane Rotation Barrier Nerfed?
Ethane got hit with the nerf hammer! The rotation barrier dropped from 12 kJ/mol to a measly 8 kJ/mol. This is basically the molecular equivalent of your favorite character getting downgraded in a video game patch. The devs clearly thought those methyl groups were rotating too slowly and needed a mobility buff. Next update: watch them nerf cyclohexane's chair-boat interconversion because too many students were actually understanding it.

Poor Cyclohexane Gets Structurally Friendzoned

Poor Cyclohexane Gets Structurally Friendzoned
Dating in the chemistry world is brutal. Poor cyclohexane tries to match with someone who's looking for "a guy like this" while showing a boat conformation drawing. The irony? Cyclohexane IS literally that structure—just drawn in chair conformation instead. It's the molecular equivalent of being rejected for wearing different clothes when you're the exact same person. Chemistry students everywhere just felt that burn in their C-H bonds.

2D All Day Baby

2D All Day Baby
The eternal struggle between idealized chemical structures and reality! On the left, we've got that perfectly symmetrical benzene ring that organic chemistry textbooks love to show us. On the right? The actual chair conformation of cyclohexane that makes undergrads question their life choices. Just like the cartoon faces below - expectation vs. reality. Your professor draws that pristine hexagon, but when you try to visualize the actual 3D structure with those awkward axial and equatorial bonds... suddenly chemistry isn't so flat anymore. Turns out dimensional reality is just disappointing all around.

Dogs Explain Molecular Conformations

Dogs Explain Molecular Conformations
Whoever created this organic chemistry textbook deserves a Nobel Prize in educational illustrations! Using dogs to explain molecular conformations is pure genius. The stable conformation dog stands normally while the unstable one is doing a ridiculous headstand—exactly how molecules behave when they're energetically unfavorable! And those different configurations with backward-facing dog heads? Perfect representation of how cis-trans isomers have different spatial arrangements but can't convert without breaking bonds. Chemistry students everywhere are simultaneously learning and questioning their sanity. Next chapter probably explains reaction mechanisms with cats knocking things off tables.