#enantiomers
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I was at the Snohomish County EMS conference yesterday and there was a super interesting lecturer named William Heuser, he is a clinical pharmacist and toxicologist, as well as a critical care flight paramedic. I was warned ahead of time that the lecture would "knock your socks off", but was surprised because he spoke like a fire and brimstone Pentecostal preacher but he was yelling about about traumatic brain injuries and intubation sequences medications. It was so cool, after the lecture I go up to him and ask "Can you autograph my chemistry homework? It the only thing I have available."
He said yes, and then glanced at the paper and said "Oh, you are learning about ecgonine - you must be studying Organic Chemistry."
Me: "Yes, it was exciting during your lecture when you brought up s-ketamine vs racemic ketamine I was like "oh he is talking about enantiomers!""
Him: "You know what enantiomers are! I trained in Oganic Chemistry so I think that's awesome, most people don't want I am talking about. Good luck on your studies."
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The maximum number of stereoisomers possible for this molecule is 2ⁿ = 2² = 4, each of which is drawn in figure 17.20.
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"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.
#book quote#chemistry#nonfiction#textbook#trihydroxybutanal#stereoisomers#enantiomers#erythrose#threose
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Again, 2-methylcyclohexanol has two stereocentres and exists as 2² = 4 stereoisomers, with the cis isomer as one pair of enantiomers and the trans isomer as a second pair:
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"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.
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Gonna start using enantiomer terminology to talk about everyday chiral objects.
Ugh, all our bread knives are R configuration. I wish we had a racemic mixture so I could pick a knife with the right chirality to actually use the serrated edge without having to cut towards myself.
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Chiral Separation
Chiral separation is the process of separating enantiomers, which are mirror-image isomers of a molecule that cannot be superimposed onto each other. Enantiomers possess identical physical and chemical properties but exhibit different biological activities. Chiral separation is crucial in fields such as pharmaceuticals, agrochemicals, and fine chemicals, where the specific enantiomeric form of a molecule may have different effects or interactions in biological systems.
Types of Chiral Separation
Preparative Liquid Chromatography System
The Hanbon preparative liquid chromatography system finds widespread application in the separation and purification of a diverse range of substances, including pharmaceutical intermediates, biopharmaceuticals, synthetic drugs, natural products, fine chemicals, and food additives.
Chromatographic Column
Hanbon offers a range of medium and high-pressure chromatography columns, including laboratory columns and DAC (dynamic axial compression) columns.
Simulated Moving Bed (SMB)
In 2005, Hanbon introduced the innovative DAC® (dynamic axial compression) column, which incorporates iSMB (simulated moving bed) technology.
Continuous Ion Exchange Chromatography
Continuous dissociation technology is a powerful combination of standard fixed resin bed technology and continuous counter-current systems.
SFC (Supercritical Fluid Chromatography)
Supercritical Fluid Chromatography (SFC) is a powerful chromatographic technique that utilizes supercritical fluids as the mobile phase.
How Does Chiral Chromatography Work?
Chiral chromatography relies on the use of a chiral stationary phase, which is a solid or liquid material capable of differentiating between enantiomers. The chiral stationary phase interacts selectively with the enantiomers, leading to differences in their retention times or elution orders. This separation is based on the differences in their molecular interactions, such as stereoselective adsorption or formation of inclusion complexes.
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I wonder where the name Meridia came from. I'm reading about Meridional energy transfer, the transfer of energy from the equator, North and Southwards to the poles along a gradient. And that sounds similar to her sphere. :0
#there's lots of almost sciencey tidbits if you look hard enough#When I took molecular bio I remembered what Enantiomers where because of the Enantiomorph#Which one of the devs said actually was not the inspiration but it helped me regardless
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bingge vs. bingmei
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I’ve been on spring break recently, so there wasn’t much to post.
Studying for my second exam, and I’m really struggling with enantiomers and meso compounds. Any tips? I feel like I’ve watched every video on the subject.
#organic chemistry#study aesthetic#studyspo#studywithme#aesthetic notes#gel pen#notes#study#study hard#study motivation#studyblr#studyspiration#academia#homework#isomers#enantiomer#diastereoisomer
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beautiful lesson at smelling class
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ochem is the funniest subject. why did they call it a backside attack
#every time i see glass and allison’s icons on discord i think of enantiomers -> then i think of ochem -> lol backside attacks#wheres my nucleophile joke
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The trans isomer is chiral and exists as a pair of enantiomers.
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"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.
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A classic example of a coordination complex (see chapter 13) that can exist as enantiomers is the golden-yellow [Co(en)3]³+ ion (figure 17.13).
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"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.
#book quotes#chemistry#nonfiction#textbook#ethylenediamine#cobalt#coordination complex#enantiomers#golden yellow
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Similarly, 3-methylcyclohexanol contains two stereocentres and exists as 2² = 4 stereoisomers, with the cis isomer as one pair of enantiomers and the trans isomer as a second pair:
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"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.
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hey guys ! very unfortunately, i'm entering midterm week so two-faced updates will be super inconsistent across the next few days. i will try to update as much as i can but i'm worried if i do, then all the chapters will be about organic chemistry or anatomy so. yk.
think of it like gojo n the gang are also going through their midterms so they do not have time to go on twt (soon to be called x like wtf is that) and be silly
thank you for all the love on two-faced as always !! love u guys 🤍
#( 🗣️ ) — en talks#thinking abt chem so much that my little activity graph on the side is starting to look like an alkane#if there was a halide on the end it would a primary alkyl halide#that means sn2 mechanism reaction#also meaning it would react w nu to form one enantiomer#bc its sn2 the reaction would take place in one step (the rds) meaning the rate equation would b#r=k[eu]#to determine if this was sn1 or sn2 if u didn't know alr u could do an experiment where you reacted the alkyl halide w the nu and then anot
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