Sometimes, it's helpful to decompose a complex field into the most useful categories and perspectives so you can attack difficult problems more easily. It's an interesting exercise to see how well you understand the foundations of such and such field, as well as figure out whether there are parts that you do not understand well.This is how I would frame the different levels and angles of chemistry, if I had to balance between simple and yet comprehensive:
>Chemical/Physical Properties Subatomic/Electronic Atomic Bonding Molecular Material >Thermodynamic Constraints & Equilibrium Kinetic Energetic Entropic >Chemical Interactions Types of Reactions Reaction Mechanisms Systems of Reactions
i'd break it into lab and lecture and skip the one that doesn't take attendance
Andrew Campbell
By systems of reactions do you also mean in living systems? Beacose that's what i'd add.
Isaac Perry
I think so. It's definitely something I want to cover. I almost want to break up reaction mechanisms to include both the molecular components (is it nucleophilic? electrophilic? etc.) involved and the step-by-step processes (what are some competing lists of reactions that get to the product? what happens if you add a catalyst? etc.).
But otherwise I'm quite satisfied with what I have here. Think about to the idea about nucleophilic substitution. Is it one of the various "reaction mechanisms" that can happen? Yes. How can you tell? Look at its chemical/physical properties. Will it happen? Study the relevant thermodynamics.
Luis Brown
u should never make anyone ever memorize reactions. its a waste of time and there are infinite numbers of them. useless prep for the mcat or any actual science
Nathaniel Kelly
Now here's a man with PRACTICAL IDEAS.
Carson Brooks
Who's making anybody remember reactions?
I think I might edit the Chemical Interactions category to reflect the difference between getting an intuition of what all of the steps from reactants to products in more complicated reactions may look like and the kinds of active molecular components (functional groups, atomic properties, etc., that lead to nucleophilic attacks, etc.) that drive reactions.
At the most simplest level, it's just talking about the limited combinations of reactants/products possible in a single step, i.e., synthesis, decomposition, single replacement, double replacement, or reduction/oxidation. Of course, as you get into more complicated reaction mechanisms, there are potentially unlimited amounts (accounting for every series of possible reactions that get you from reactants to products), but you can still get a good intuition of the basics.
Jace Hernandez
they made me when i went through organic, i had too memorize 50-60 for each test, it was poop
Carter Long
Also I would add acid-base reactions to the type of reactions, since I thought to myself at first that acids and bases could be explained as one of the 4 basic "building block" reactions or as a reduction/oxidation reaction until I realized that some acids are counterintuitive.
Nicholas Phillips
>his lectures take attendance
hahahahaha
Brody Brown
Speaking of Sn reactions. I bought this document from masterorganicchemistry a while back and it proven itself to be quite usefull.
Alexander Sanchez
I found that for myself, keeping things such as electronegativities, polarizability and spacial awerness of the molecules in mind when working with reactions helps alot.
Colton Baker
Yeah. I think you can classify that under "Molecular" chemical/physical properties. properties.
Ryan Roberts
bump
Jacob Perez
t. premed
Carson Cox
bumperino
Jack Sanchez
>I almost want to break up reaction mechanisms to include both the molecular components (is it nucleophilic? electrophilic? etc.) involved Check out Ian Fleming's book on frontier orbitals. The "electron-pushing" heuristic for polar reactions is really just a convenient shorthand for the qualitative behavior of waves
Connor Butler
Cheers
Aiden Gray
I find myself using the top one much more. The bottom one makes it look like those electrons are completely off limits.
Anyways, does anybody here know what would happen visually if you made a polyurethane?
Grayson Myers
>core intuitions wat
Hunter Myers
All chemistry can be subdivided into two groups:
A- making drugs
B- making bombs
Justin Reyes
you know, basic shit that helps you think about more difficult shit that you kinda just know from studying hard
Eli Cooper
this chart really helped me alot as a christian trying to learn chemistry my parents don't want me to go to college for chemistry because they say it's indoctrination and it'll turn me gay and a socialist, so they bought me physics text books by kent hovind instead
Connor Richardson
Yeah, i watched a few lectures on the subject and i've got to say, it's the modt elegant and explenatory model of chemical interactions i know of..
And i finally know why activation energy is higher than intermidiate in sn reactions, never thought of antibonding orbitals before.
why did they rename all the elements ?, seems needlessly confusing >magnesium,neon,sulfur.indium,hassium all share the same letter >selenium,iodine,gold are just a fucking line
do they hate mendeleev or something ?
Aaron Nguyen
Read the table as you would a sentence, autist..
Jackson Fisher
how the fuck is a periodic table a sentence ? also in that pic they made the new names of all the elements fucking microscopic so i cant read it, only the new letters they gave them.
Adam Martin
Read the table as you would a sentence, autist >WhEn He MaDe ThE WoRlD GoD ...
Anthony Gomez
that's not how you read a table you dumb fuck i can do the same thing HHe Li BeB CN OFNe NaMg
stringing together atomic symbols like that dosnt make sense, especially since it dosnt correspond to any chemical like OH or NaCl or something.
Jason Rivera
>Ian Fleming
--
On topic: seems like you can classify that easily under "bonding/structure" if you can nudge that between the chemical/physical properties of atoms and molecules in that list.
Nathaniel Miller
>i can do the same thing you did it!
Adrian Barnes
yes but what does it mean? what is 'HHe' or 'OFNe' im pretty sure such chemicals have never been observed .
Jackson Taylor
What the fuck are you on about?
Total AuTiSt
Nathan Martin
Professors never really seem to tire of that joke. Like, it's not terribly original, but it just gets funnier every time you hear it.
Anyways, it's a very elegant interrelationship between structure and reactivity. You can predict/rationalize a fairly wide range of reactions and regioselectivities with HOMO/LUMO tables. Or today, fast HOMO/LUMO calculations in your computational chemistry software package. Include the other orbitals and you get a better result as well. There's a really massive amount you can go into on just bonding/electronic structure, say in quantum chemistry, but the mathematical overhead is huge for non-specialists and there's a lot of ground to cover while you get bogged down in seemingly trivial results and autistic formalism. If you like math it's a good idea to go beyond the "undergrad pchem" material into some of that, but the true beauty of frontier orbital theory is how much it achieves with very little math. Look more at computational chemistry if you want to "bridge" electronic structure with reactivity, reaction pathways, mechanisms, kinetics/dynamics, etc. at a more nontrivial level
Oliver Richardson
Thank God that the chemists are here today. I was afraid that my thread wouldn't generate any valuable discussion. Thanks for the book recommendation, I'm not quite there yet, but I hope to be after this year's courseload.
> Look more at computational chemistry if you want to "bridge" electronic structure with reactivity, reaction pathways, mechanisms, kinetics/dynamics, etc. at a more nontrivial level Is there any reason why this is reserved for "computational chemistry"? Sounds like this would just be physical chemistry or maybe one of the other specializations unless it requires modeling. Am I just misinformed on what computational chemistry entails?
Daniel Cook
>Fleming's science and mathematical texts are top-notch. My first exposure to his work was when I was given a copy of "Casino Royale," a book on casino probabilities and card-counting. While it was a little out of my field, learning about systems like High-Low as well as Effect of Removal definitely improved my understanding of on-the-fly statistical projections. A few years later, I read Moonraker for a course on orbital ballistics - this was much more my speed, and I learned a great deal about hyperbolic and parabolic trajectories. More recently, I read (mostly for recreational purposes) "Chitty Chitty Bang Bang," which, while aimed at a juvenile audience, still greatly enhanced my knowledge of internal combustion engines - hey, I'm a rocket surgeon, not a mechanical engineer. His most recent text, "Frontier Orbitals and Organic Chemical Reactions," while less imaginatively-named than his earlier works, still facilitated my understanding of peroxide-based liquid fuels and how to correctly predict outer-shell orbital interactions as well as electron pushing for that murky area between the organic and inorganic fields of chemistry, oxidation. From Amazon reviews.
where are my autistic chemists at? r8 my simple heuristics system
Wyatt Lee
you should bump this shit, like they do in the future
Matthew Wood
>Is there any reason why this is reserved for "computational chemistry"? Sounds like this would just be physical chemistry Well, computational chemistry -is- a pchem field. It's just more applied, and concerned with connections to more broadly relevant chemical properties/phenomena. That, and it refers more to the methods you use, emphasizing calculations over formalism. Pchem is a huge topic, you have both "chemical physics in general" and "chemical physics how they pertain to their specific emergent properties"
Daniel Perry
this
Dylan Sanchez
bump
Jace Gonzalez
I guess all of the chemists are busy doing their natural product syntheses and don't feel like commenting on the summaries of a pleb like me. It's okay, I understand.
Tyler Reed
this should help you for 3 weeks of first semester organic
Mason Adams
Have fun drawing a Kolbe carboxylation with that retarded representation. Or explaining activating/deactivating effects.
Connor Ramirez
>implying carboxylation can't be explained through atomic properties, molecular structure, bonding, active functional groups and how they contribute to reaction mechanism, how heating is required due to thermodynamic constraints, etc. Brainlet premed detected. Go memorize and regurgitate somewhere else.
Adrian Diaz
what's the meaning of OP's picture?
representing the electrons as delocalized is more akin to reality?
Ryder Foster
>like commenting on the summaries of a pleb like me >r8 my simple heuristics system Where? Have you posted this yet?
Ryan Thompson
Read the OP.
I hate drawing lines. Circles are quicker and don't expose my terrible handwriting as badly.
Brayden Stewart
he was talking about the "delocalisation curve" retarded-circle-in-hexagon benzene representation you brainlet
Juan Gomez
It's both less intuitive for mechanisms and harder to draw.
Julian Edwards
Oh, you're right. My bad. Now I look like an asshole.
Justin Jones
>Read the OP. But I don't see any heuristic there, all you've done is clumsily try to partition the field
Isaac Wright
Is it that clumsy? I've finished general chemistry and my first semester of organic chemistry, and I thought that it would be a good idea to see what I've learned. These seem to be the most general, simplified dimensions to look at when understanding chemical reactions, and more nuanced and specific phenomena, such as molecular orbital theory, VESPR, catalysis, functional groups, etc., can be classified under one of these categories.
Owen Cooper
>Is it that clumsy? Yes.
I see what you're trying to do, and it might work when it comes to teaching the material in a basic chemistry class, but real chemistry problems usually can't be partitioned that easily.
Taking a really basic example, you run a reaction and you end up with a precipitate. If you try to approach the problem from only one angle, say polarity, maybe you'll figure "the reaction was run in water, so clearly I made something non-polar that's not soluble in water." That's great, except >Maybe you made crystals >Maybe your compound IS polar, but still not soluble (like lead iodide). >Maybe your compound cooled down resulting in a lower solubility causing the compound to crash out.
There are ways of approaching problems to make them simpler, but all of chemistry is interrelated and you can't really just look at a problem from one approach and expect that to be right (unless you're taking a test and it says "now consider this approach...")
Robert Powell
Okay. That's a fair and helpful criticism. Now I don't mean to use this little writeup to categorize chemical reactions as one-dimensional. Instead, I want to consider multiple factors at once, since any of these categories could be involved in chemical phenomena, so you have to consider each angle for a full understanding depending on the problem. Do you think it's still an issue?
Aiden Hill
but he said literally the opposite
Chase Rivera
Why would anybody make a list like this only to limit themselves from considering one concept of chemistry at a time? Seems useful for remembering to examine a particular reaction from multiple angles in order to understand it.
Dominic Walker
bump
Oliver Sanchez
>my parents don't want me to go to college for chemistry because they say it's indoctrination and it'll turn me gay and a socialist
Should have reinforced that you were doing chemistry and chemical engineering
John Bailey
>not already gay and socialist spot the brainlet
Jeremiah Thomas
bump
Aaron Garcia
You shouldn't draw your benzene rings like this, it can lead to mistakes (e.g. drawing impossible structures of polycyclic molecules)