« first day (2798 days earlier)      last day (2140 days later) » 

Anonymous
5:00 PM
He also has a few lectures on Measure theory and Lie algebra...if you're interested in that kind of stuff
 
I feel sleepy
 
Anonymous
(haven't watched those yet)
 
@ACuriousMind Huh, I guess I misunderstood it. Then we have a good definition of math, i.e. defining the axioms as true and deriving true statements from them, right?
 
What's the definition of math?
 
@SirCumference I think you'll find that except for logicians and other foundationalists, mathematicians rarely view math in those terms
 
Anonymous
5:01 PM
Anyhow, as Balarka says, probably you're better off learning multivariable calculus first
 
@Danu I would enjoy learning about these topics, but I would also like to learn about h-principles before I grow into a mathematical recluse.
 
Anonymous
and build on linear algebra
 
Anonymous
Then you could take basic analysis....not a good idea to jump onto advanced topics directly without background
 
@heather I think there's not really a point to that. h-principles is a pretty advanced thing.
 
@heather Learn linear algebra before multivariable
 
5:02 PM
I mean, the algebraist that introduces group theory may pay lip service to the axioms by mumbling something about e.g. the axiom of choice, but the practice of the subject rarely involves the actual axioms
 
(for example, I'm not too confident I could quickly learn how to use them, and I'm a math phd student)
 
@Danu i suppose, yeah. it just seems interesting.
 
I think one could write a Mathcamp course notes on h-principles for high schoolers tbh.
 
@Semiclassical "While de Broglie presented a first order development of the quantum trajectories (integrated from the velocity), Bohm himself did a second order (integrated from the acceleration) emphasizing the role of the quantum potential. The differences between both approaches appear when one considers initial ensembles of trajectories which are not in quantum equilibrium. Except for this issue, which will not be addressed in this book, both approaches are identical"
 
But there just isn't one
 
5:03 PM
and @Balarka's explanation made sense so far, so I wanted to keep going.
 
How big a deal is that
 
Well, as it says, it depends on your take on quantum equilibrium
if you assume that's true, then there's no practical distinction at all
 
@heather There really is no "intro to" h principles. They are a relatively recent and deep and hard branch of mathematics and the texts are usually unreadable. I am filtering through the perspective I have gathered on it over the course of months of reading those.
 
@BalarkaSen can you use the h-principle to solve the hypergeometric equation or equations like that?
 
@bolbteppa why would you want to
 
5:04 PM
You can't use the h-principle on everything lol
 
Does the Banach-Tarski paradox disprove the axiom of choice
 
there's a reason why we love series solutions, lol
 
@BalarkaSen well yeah. i'm not saying it was a reasonable wish =)
 
There isn't anything wrong about the wish either!
 
I gave up and am just trying to relate everything to hypergeometric equations now :(
 
5:05 PM
It's cool math
 
@enumaris No. Btw dropping the axiom of choice also produces some weird effects. Lemme search the transcript....
 
@bolbteppa You should work on electro-magnetic duality in N=2 supersymmetric gauge theories
 
@bolbteppa Painleve 4 lyfe
 
there's hypergeometric series EVERYWHERE
 
@Danu I think that's mostly because periods of riemann surfaces show up everywhere in there
 
5:06 PM
Once I write up the notes on this, going to go over Lame equations and Painleve (again ffs)
This stuff is insane
 
and periods of riemann surfaces generically satisfy picard-fuchs equations, which are hypergeometric (or appropriate generalizations thereof)
 
Yeah, probably
 
in particular you don't get equations with irregular singular points
 
how can you make 2 copies of a ball from 1 ball tho that's just weird yo
 
hence the usual series solutions have a hope of working, with the only possible issue being log terms
 
5:07 PM
@heather If you want to read some cool topology without having to go down the rabbithole, try Colin Adam's "Knot Book".
 
I can't imagine what you'd do with equations which don't have at most 3 regular singular points :p
 
I haven't gone through it thoroughly, but I have heard very good things about it.
 
@enumaris E.g. without choice, the dual space of a vector space can be the zero vector space! An infinite-dimensional vector space without any non-trivial linear functions on it is also just weird.
 
okay. well thank you =)
 
eh. i've dealt with equations that had more than three :)
 
5:08 PM
If you read it I'll probably too.
 
though tbh I very much relied on mathematica being able to solve them, at least in terms of generalized hypergeometric functions
 
In mathematics, Riemann's differential equation, named after Bernhard Riemann, is a generalization of the hypergeometric differential equation, allowing the regular singular points (RSPs) to occur anywhere on the Riemann sphere, rather than merely at 0, 1, and ∞ {\displaystyle \infty } . The equation is also known as the Papperitz equation. The hypergeometric differential equation is a second-order linear differential equation which has three regular singular points, 0, 1 and ∞ {\displaystyle \infty } . That equation...
This is like Hypergeometric's father
 
@enumaris The essence of why the B-T paradox works is that the "cutting" maps do not respect the notion of "measure" or "volume", and hence you shouldn't expect them to preserve volume to begin with
 
@DanielSank I think the matrix is a bit of a red herring brought about by the representation
 
5:09 PM
I think you're just seeing the fact that $a$ is an eigenfunction (in the classical case!) of the operator $\{H, \cdot \}$.
 
hmmm
 
@BalarkaSen i might give it a go then.
 
how catastrophic would it be if we had to get rid of the AC?
 
i'm looking it up and it seems interesting.
 
@EmilioPisanty I see we agree ;)
 
5:13 PM
losing the axiom of choice will also make analysis very unwieldy, such as losing baire category theorem
 
15
Q: Hahn-Banach without Choice

Mark KimThe standard proof of the Hahn-Banach theorem makes use of Zorn's lemma. I hear that, however, Hahn-Banach is strictly weaker than Choice. A quick search leads to many sources stating that Hahn-Banach can be proven using the ultrafilter theorem, but I cannot seem to find an actual proof. So... ...

I think you would lose things like HB
 
It's really a small cost to pay to have nonmeasurable sets due to axiom of choice, then to deal with a whole wilderness of non well orderable sets without the axiom of choice
(I am fine with either btw)
But it is quite a big deal to lose baire category theorem
(and trust me, I am pretty sure nature can never really demonstrate the existence of a nonmeasurable set)
 
Is a set smaller than the plank length measurable or non-measurable? runs
 
It will probably be buried in the noise for that measurement to be meaningful, I think
 
@bolbteppa Mu
 
5:18 PM
so it probably will not have physical significance
 
okay, wow, this knot book is cool
 
It is seriously cool
 
hmmmm
tough questions
crap, my script is now a throwing an error where it didn't used to throw this error...
those errors are hard to fix -.-
time dependent errors lol
 
Anonymous
@enumaris Heh...had one like that around two weeks back. The same program when executed the first time gives the correct output but when run the second time doesn't give any output at all (on the third or fourth run it again works!). Later realized that it was a POSIX incompatibility on Windows :P
 
@heather This book actually has a lot more than I anticipated. If you read it that'll be fantastic.
 
5:25 PM
@Blue i just have a normal bug, in the sense that it is not time-dependent but i still have no idea what's going on =)
@BalarkaSen okay. it's very readable/interesting, so i think i'll read through it all =)
 
I think my query is too long
I want to pull 10k different things, so I have a "WHERE ID IN (?,?...,?)" kind of statement...
where there's 10k different ?'s
probably SQL is throwing an error saying that's too many
hmmmmm
any SQL experts in here? :P
 
Anonymous
@enumaris Are you afraid of asking on SO? :P
 
Anonymous
(I am)
 
well I don't want to ask a vague question
 
Quantum non-equilibrium is a concept within stochastic formulations of the De Broglie–Bohm theory of quantum physics. == Overview == In the Copenhagen interpretation, that is, the most widely used interpretation of quantum mechanics, the Born rule ρ ( x , t ) = | ψ ( x , t ) | 2 {\displaystyle \rho (\mathbf {x...
 
5:30 PM
generally when I post to SO it's like a very concrete 1-step answer kind of question
 
Is that what they mean about equilibrium in the quote above
 
Anonymous
@enumaris Same here. I used to get a question ban almost everytime there :P
 
Is that the De Broglie-Bohm equivalent of the Quantum Kinetic Equations?
 
@Blue i don't go over there very often; it's always rather frustrating.
(except when just googling; i mean to ask a question.)
 
5:31 PM
the "predicted properties" in that section is worht looking at
 
Anonymous
@heather They seem to be waiting to pounce on you and downvote you $24\times 7$ ;)
 
as far as reasons I find the notion of quantum non-eq to be distateful :P
 
Anonymous
And sometimes even non-duplicate questions get closed as duplicates (of a vaguely related question)
 
'thereby violating the assumption that signals cannot travel faster than the speed of light'???
 
yea...
 
5:32 PM
If he's doing non-relativistic QM that's not a problem right
 
Anonymous
I have some serious appreciation for those who manage to get 10k+ rep there on SO
 
well, I think it'd let you do nonlocal signaling instead of just nonlocal correlation
standard QM (and as such equilibrium BM) lets you do the latter but not the former
 
@enumaris Surely there's another field that you can use the WHERE on if it's that many? The only other thing I could think of would be to select them all and filter in your code or run 10k selects with the individual ids
 
@Blue basically, yeah. it's weird. a really simple, sometimes bad answer with just code pasted in gets 10 upvotes, but a good question gets 10 downvotes with "trivial" or "read the docs" in the comments.
 
There are alternatives
but I worry that the alternatives will miss stuff
 
5:35 PM
Al + O2 = Al2O3 Why does Al stay without an index and why is the index of the oxygen 3? I mean, I know this is pretty basic but has been bugging me for a while. Why isn't it Al2 + O3 = Al2O3?
 
I can filter on a date for example, do something like date>something, but then I might miss a few rows
 
I'm not totally clear on this stuff tho
 
the way I have things set up right now looks at one table and matches another table and pulls the indices of one table that doesn't appear in the other, and then I select all those indices out...which is why there's 10k+ of them
pulling by index
individual index
so it's basically "WHERE INDEX IN (INDEX1,INDEX2,...,INDEX10000...)"
 
Can't you just do the select in that query if it pulls the indices?
 
hmmm
lol duh
I guess that would be the way to go
 
Anonymous
5:38 PM
@heather True, yeah. And the "rude comment" thing seems real when you go there. Any simple "Did you even read the documentation?" comment will get 10+ upvotes, even when it is extremely hard to dig up the required detail from the documentation as a beginner. I guess that prevents the homework vampires though. Anyhow, the chat rooms on SO are somewhat more helpful.
 
Anonymous
Especially the Python chat has some helpful folks hanging around
 
I think my brain didn't go that route cus I'm only pulling stuff from one of the joined tables
 
How does that relate to normal QM density matrices
 
so it seems a bit weird mmmhm
 
5:39 PM
No idea. But the $\rho$ in there isn't a density matrix, it's just the probability density as a function of position
 
@danielunderwood thanks :D
 
I'm sure there's stuff in the literature on this, but I steer clear of that so I can't help
 
@Blue yeah, i had a bad experience in there a couple times, so i haven't been over there for a while.
but in general that chat is more helpful than most of SO, yeah.
 
@enumaris It's not an unusual pattern to join two tables and then only read fields from one of them (or even only shared fields).
 
5:41 PM
That has some comments by Einstein, Pauli, Heisenberg on Bohm
 
yeah
including Einstein's remark to the effect of it being too cheap
 
@ACuriousMind yeah, but it's just the way my brain logics
 
@Danu :) I just meant what little I have came in contact with(and it's mostly algebra and basic geometry), but yes you are correct, I don't think I have a lot of knowledge. If I manage to get to the program I'm currenlty studying for, topology won't be the first think to learn. As for LMU, I also have it in mind.
So, thanks for your opinion.
 
Cool
 
Or joining 10 tables if the db schema wasn't set up for use lol
 
5:43 PM
well I'm no SQL wiz
 
@danielunderwood on that note, a title I saw randomly the other day (but didn't follow up on)
 
This is actually my first time using a LEFT JOINlol
 
@Semiclassical there's a hat stack exchange?
 
yeah, but it's only open during the holidays
 
5:44 PM
Also: thanks SE for the very nice Stack Overflow nalgene bottle
 
hahaha
the title of what i linked, for those who didn't look: "Relational Databases and Bell's Theorem"
I mean what
 
are they building Relational Databases using entanglement now?
 
@enumaris are you sure you want a left join?
 
like if your row changes in one database, it should change accordingly in another FTL? :P
@EmilioPisanty pretty sure, I am finding all entries in one table that doesn't have a corresponding set of entries in another table after all.
 
I mean, I reckon some 50% of all left joins out in the wild could just as happily be straightup joins
@enumaris I.... don't think that's what left join does?
 
5:47 PM
huh, the stuff they do in the middle of the paper (past the horrible category stuff) actually looks like the kind of argument I've been doing lately
 
you might be able to manipulate it into that
 
Left join, afaik, takes all the entries of the left table and all matching entries
 
@Semiclassical Well that's something I never thought I'd see. I think relational databases have pretty strong mathematical background that's related to set theory, but I don't know the technical details
 
@enumaris yes
 
it fills the right table's columns with NULLs where there isn't a match
 
5:48 PM
when the latter exist
@enumaris yes
 
so I do a left join and find where all the NULLs are to find rows in the left table that didn't match
then I pull the left table's contents
 
@EmilioPisanty Shouldn't all left joins (or right or inner) be happy as normal joins? The left/right/inner just return less and have better performance I thought?
 
@danielunderwood I've never fully understood
 
"In database language, this says exactly that there is no ‘universal relation’ on the whole set of attributes which yields each of the ‘observable relations’ by projection"
 
by "normal join" do you mean outer join?
cus by "normal join", I'm thinking of an inner join lol
 
5:50 PM
but as I understand it, on that $A \setminus B$ diagram, you'd be just as happy using join instead of left join
@enumaris no, just join
 
since that's the kind of join you get if you type something like "Select a.x,b.y from a,b where a.x=b.y"
what's "just join"?
 
I'm actually not sure what join is. I thought it was normally the same as an outer, but I wouldn't bet on it
 
SELECT
  questions.Id AS [Post Link],
  cast(questions.CreationDate As Date) AS 'date',
  initialQs.Id AS [Post Link]
FROM Posts questions
JOIN Posts initialQs
no surname needed
 
isn't that an inner join
 
5:51 PM
"In particular, we shall see that the question of whether an “empirical model”, of the kind which can be obtained by making observations of measurements performed on a physical system, admits a classical physical explanation in terms of a local hidden variable model, is mathematically equivalent to the question of whether a database instance admits a universal relation"
 
there's only 4 possible joins right
 
Woah I didn't know there was an SE data explorer
 
@enumaris ¯\ _(ツ)_/¯
 
inner, left, right, outer
logically those are the only 4 possibilities
 
@enumaris so what's the one in my code sample?
 
5:52 PM
so a "normal join" has to be one of those lol
 
is the phrase "universal relation" one which sounds familiar to your database experience?
I have an inkling of what it measn
 
I think your code sample is an inner join...but that only returns rows where both tables have a matching entry
 
@Semiclassical not mine
 
"Here we take a universal relation for the instance by definition to be a relation defined on the whole set of attributes from which each of the relations in the instance can be recovered by projection. This notion, and various related ideas, played an important role in early developments in relational database theory [refs]"
 
@Semiclassical ugh
I was thinking tensor products but that's a universal property, innit
 
5:54 PM
lol
 
839
A: Difference between JOIN and INNER JOIN

palehorseThey are functionally equivalent, but INNER JOIN can be a bit clearer to read, especially if the query has other join types (i.e. LEFT or RIGHT or CROSS) included in it.

 
The universal relation assumption in relational databases states, that one can place all data attributes into a (possibly very wide) table, which may then be decomposed into smaller tables as needed. However, the assumption that a single large table can capture real database designs is often plagued with a number of difficulties. The "nested universal relation" model has attempted to address some of the problems and offer improvements. == References == == External links == Who won the Universal Relation wars? by Alberto Mendelzon...
 
They are functionally equivalent, but INNER JOIN can be a bit clearer to read, especially if the query has other join types (i.e. LEFT or RIGHT or CROSS) included in it.
I guess I forgot the Cross join...but in what scenario would u use that...
 
@Semiclassical lolz
 
anyways, yeah it seems a "normal join" or just saying "join" is an inner join
in my scenario I can't use an inner join because I need entries from one table that doesn't exist in another
 
5:55 PM
loll, that external link
 
@enumaris fair enough
@Semiclassical lolz
I don't know why that wasn't obvious to me from the title
 
crap, I can't comment in a json file -.-
 
I sorta get what they're saying, insofar as it's a question about counterfactuality: whether every possible measurement has a well-defined value even if it's not actually measured
 
@enumaris sure you can
it might impede a machine from reading it, I dunno
but you sure can
just take a crayon and write on your screen
 
5:58 PM
5695
Q: Can comments be used in JSON?

Michael GundlachCan I use comments inside a JSON file? If so, how?

 
I'm sure work won't mind
 
lol
 
maybe a felt marker is better
 
I appended a date to it to tell me when the file got appended
 
It jives with the semi-slogan I've had lately: That bell's theorem is all about whether you can impute $\pm$ values to counterfactual measurements in a way that preserves the correlations.
 
6:00 PM
but it don't work
 
@enumaris that sounds like a classic XY problem - why do you feel the need to comment a file that's usually only read by machines?
 
the file is human readable
and I read it sometimes
I guess I can find another format
but that would result in me modifying my code to accept this other format lol
 
Just add an "appendedDate" property to the object? Or grab the timestamp of the file
Or write a custom JSON parser that will allow you to comment :D
 
Well, it's human-readable (that's much easier to "debug", after all!), but it isn't intended to be read by humans
 
I have multiple appends happening on multiple days
I'd like to know what data was appended on what date
I mean, I know there are ways I can solve this
but
just not as simple as I thought
 
6:02 PM
If you want to preserve some information, just include it as an actual field and ignore it when parsing the file
 
by writing a line lol
 
[{"date": timestamp, "data": {...}}, ...]?
 
(With the basic conclusion being: It's always possible to impute values to counterfactuals in such a way as to preserve the correlations, but it's not always possible to do so by only using $\pm 1$ values)
 
36
Q: We'd like your feedback on our new Code of Conduct!

Tim Post tl;dr: We've put together a code of conduct (CoC) that is a bit more comprehensive than our existing be nice policy because we feel that our current policy isn't meeting our needs. Some background, our reasons for doing this and a link to the draft can be found below. We'd like your feedb...

 
(blah blah blah blah)
 
6:03 PM
SE's looking at a new Code of Conduct, and would like your feedback ^^
2
 
yeah all solutions require me to modify more than one line :P
 
(Anyone mind starring the second of those messages? If one stars the first it'll just show up on the board as the url, which probably won't entice anyone to look.) (Thanks!)
 
Or instead of appending, you could create new files with the timestamp as filename
 
@Semiclassical Uh...isn't "imputing values to counterfactual measurements" just another name for "realism"?
 
yep
the point is more the local vs. nonlocal bit
 
6:05 PM
@danielunderwood yeah...but then I'd end up with too many files eventually
 
I can ramble on about what I have in mind but I'm not sure that's wise :P
 
it's not essential that I know the date the data was appended on
I'll just leave it lol
oh wait
shoot, the json saves one giant dict...if I append now I'll have multiple dicts...hmmm
ok I think the way I have it set up won't work lol
welp, got some more work to do...no biggie
there's other failings that I found as well
good thing I saved multiple backups of the master file this time so I don't have to rerun 20 hours of analysis :P
 
Guys, I know there are some elements like hydrogen, oxygen, bromide... that can't exist alone so we write them with index 2. For example Al + O2 -> Al2O3 (this is unbalanced tho) and here we see that oxygen is written with index 2 because it hardly can exist alone. My question is, why chloride (Cl) (which is one of the elements that hardly exist alone) is alone in Na + Cl -> NaCl?
 
You also have H2O
where O is now alone
 
H2 + O2 --> H2O (unbalanced) is the reaction?
Where O is not alone.
 
6:15 PM
the answer is elements that "don't like to be alone" are those that bond with other atoms. In the case of Oxygen, it can bond with itself to form O2 or bond with Hydrogen to form H2O.
 
HO^- + H^+ ->H20 is the more typical one
 
Are you asking about how salt is actually created? I don't know the reaction generally used to "create" salt.
 
The index is dependent on the reaction, not the element. Na + Cl -> NaCl is with ions if it is. But I think $2\rm{NaOH} + \rm{Cl}_2 \to 2\rm{NaCl} + \rm{O}_2 + \rm{H}_2$ would be more typical
 
the general answer is "there is no hard and fast rule about what to "write and index 2 on" for chemicals and chemical reactions
^mismatch quotes error
I'll let you guys feel the awkwardness by not editing my post
Just like (if I leave a random parenthesis around
 
@enumaris (okay
 
6:18 PM
So Na + Cl -> NaCl is actually not the typical reaction?
 
@ACuriousMind ahahahaha I beat u to it
 
dammit))
(closed yours and mine ;) )
 
lol
 
@NovaliumCompany No, pure natrium and pure chlorine are rather rare :P
 
why the hell is this count query taking 7 minutes...
 
6:19 PM
@bolbteppa btw, the discussions about Pauli and Heisenberg's viewpoints re: Bohm's work (pages 11-13) are pertinent to what we've been discussing
 
@enumaris Generally a sign either your database has died or your WHERE/JOIN conditions are poorly chosen
 
oh shoot it's cus my Python script wasn't done writing the table yet LOL
 
@NovaliumCompany Note that the one I listed may not be the typical one either, that just happens to be the one I know of
 
I think I made the two requests kill each other
 
Cool, it's interesting they say in his QM book he was claiming you couldn't get hidden variables then changed his mind
 
6:21 PM
Ok, actually, why some atoms like to bond with themselves? Like O2, H2...?
and others don't?
 
It has to do with their valence electrons
 
yeah
if memory serves he came upon it while doing stuff with semiclassical analysis? lemme find a source for that
wikipedia glosses it as such:

"His first book, Quantum Theory, published in 1951, was well received by Einstein, among others. But Bohm became dissatisfied with the orthodox interpretation of quantum theory he wrote about in that book. Starting from the realization that the WKB approximation of quantum mechanics leads to deterministic equations and convinced that a mere approximation could not turn a probabilistic theory into a deterministic theory, he doubted the inevitability of the conventional approach to quantum mechanics"
for a more direct source, see the bottom of this page (remarks by bohm himself): books.google.com/…
 
It might be useless for chemistry uses, but because it's energetically favorable. I think in the case of covalent bonding, the atoms want to have a full valence layer and share orbitals for some electrons (but I'm not 100% sure on that)
 
The question is better suited for a chemistry answer than a physics one
 
On that note, is the system of two hydrogen atoms solvable by hand?
 
6:26 PM
from a physical perspective it's like "cus the equations theoretically say so even though I've never solved these particular equations cus that would be too annoying"
 
I think the main difference between the first- and second-order formulations of pilot wave theory is what exactly one is trying to recover
 
H2 + CO2 --> H2CO3 (unbalanced). Why can't we write it: H2 + C + O2 --> ...?
 
@danielunderwood highly doubt it, it'd be a 4 body problem
 
I had that feeling. Would be a neat exercise if you could though
 
@NovaliumCompany the things on the left show what you started with
 
6:28 PM
in the second-order, one is trying to recover classical mechanics. one does that by rewriting the schrodinger equation into a form that looks like the hamilton-jacobi equation plus an extra term
 
if you write it H2+CO2 it means you started with a hydrogen molecule and a carbon dioxide molecule
 
@danielunderwood If by "by hand", you mean "has it got an analytical solution", then likely no, because this is already not the case for the ionized hydrogen molecule with one body less, cf. physics.stackexchange.com/q/266216/50583
 
if you write H2+C+O2 it means you started with a hydrogen molecule, a carbon atom, and a oxygen molecule
 
which if nothing else gives a nice way to recover the classical limit: if this term is small enough to be neglected, then you're done
 
@NovaliumCompany you can write whatever you want, but what you write changes the meaning
 
6:29 PM
H2 + C + O2 isn't possible? Why?
 
@NovaliumCompany Nobody said it is not possible.
 
it's possible, it's just different
 
Isn't it the same? H2 + C + O2 --> H2CO3?
 
Seems like Bohm always has at least an interesting starting point for everything
 
When C + O2 --> CO2
 
6:30 PM
it's not saying the same thing
read my comments above
 
(returning to my spiel) that doesn't mean what you've got is equivalent to classical mech prior to making that approximation. it can't, because all you've done is rewrite the schrodinger equation
 
@enumaris I read it. H2 + C + O2 would give H2CO3 woudn't it? (unbalanced)
 
it's just making it clearer where the difference between quantum and classical mechanics lies
 
Not sure if that's the chemical reaction that would generally occur
but my comments only tell you about the left hand side and why the 2 expressions differ
 
I don't know about the reaction, but I'd imagine it's not favorable. If you put in energy, you'll get some amount of H2CO3. I think most of the chemical reactions you'll see are ones that can happen spontaneous. For a bit of a different perspective, you could look into nuclear reaction branching ratios
 
6:32 PM
@NovaliumCompany Yes it would (to a very small extent, most of the stuff on the l.h.s just wouldn't react at all). But it is a different reaction than $\text{H}_2 + \text{CO}_2 \to \text{H}_2\text{CO}_3$.
 
by contrast, I take the first-order approach to be directed toward the simpler question of getting trajectories out of the Schrodinger equation
 
I know it's different, but would give the same thing?
 
not worrying at all about recovering classical mechanics, but just trying to get some notion of trajectory
 
If the reaction occurred. I imagine that combination would be happier just staying as carbon, oxygen, and hydrogen
 
@NovaliumCompany Yes, but with a different rate of reaction (likely an infinitesimally small one, I don't think you would observe significant formation of carbonic acid just when putting hydrogen and oxygen in the vicinity of carbon)
 
6:34 PM
that both the first- and second-order formulations are equivalent (subject to quantum equilibrium) reflects the fact that both of them (at least in this presentation) are extracted from the Schrodinger equation
 
@ACuriousMind Why not?
 
@NovaliumCompany Because the rate of reaction depends on how "reactive" the components are and how energetically favourable the reaction is.
It's complicated and you'll have to ask a physical chemist if you really want the gritty details
 
Ok thanks :)
 
I'm not conversant on how the two formulations differ once you break equilibrium, tho
 
And carbon on its own is pretty stable, cf. diamonds, pencils
 
6:41 PM
@NovaliumCompany if you're asking that question, you may want to look into branching ratios. I think nuclear/particle physics makes it a bit more clear that there are more possible reactions that what I've seen in chemistry. Unfortunately, I can't really find any information on branching ratios that isn't technical
Griffiths' particle physics has a decent introduction I think, but probably a little out of the way if you're interested in chemistry.

Speaking of which, what do you guys that hate Griffiths think of that book? Is there a more up to date book that people use?
 
7:02 PM
Actually you may get some explanations if you look up stellar nucleosynthesis. Most explanations probably won't explicitly mention branching ratios, but they'll give you an idea that multiple pathways are possible
 
7:20 PM
@Sid England vs Columbia is basically American football.
 
7:35 PM
-1
Q: Weber Electrodynamics

Researcher720Last year, just for the fun of it, I decided to verify (not derive) Maxwell's 4 differential equations using the scalar and vector potential function definitions of the fields. I performed the spatial derivatives on the left of each equation to see if I got the right hand side of each equation. ...

I'm out of closevotes =|
anyone round here care to take a look?
@ACuriousMind, say?
 
reading
and closed, pretty clearly non-mainstream
 
thanks for taking the time =)
also, I imagine OP and answerer are the same person?
and that they're misrepresenting their relationship to the resource they quote, too
 
@EmilioPisanty I can't really comment on accounts being related; it's better if you put such speculations in a flag.
 
I've heard people try to dispute qm and relativity, but I have to say em is a new one
 
@danielunderwood We get non-mainstream physics users on almost every topic once in a while :P
 
7:50 PM
Silly me thinking of em as untouchable
I almost feel like we could have a Dinner for Schmucks type of situation here, but that would probably just be too much to handle
 
can this question really be answered by newton mechanics?
54
A: Why don't we feel the subtle speed change of Earth's elliptical orbit?

Henning MakholmJohn Rennie's answer is right from the viewpoint of General Relativity -- but since the question is tagged with Newtonian mechanics, it deserves a Newtonian answer too. In the Newtonian framework, I think the best answer to "why don't we experience this force" is that we can't feel forces that a...

does newton physics explain how free fall frame = inertial frame (due to the Sun in the question)? I think this is a key to this question
 
'Weber electrodynamics is mathematically consistent. Maxwell's electrodynamics is not. '...???
 

« first day (2798 days earlier)      last day (2140 days later) »