@AvnishKabaj i think part (b) is based on the fact that even in sn1 the product composition is not exactly racemic but rather 55:45 in favor of inversion
"Carbons at bridgeheads, although extremely reluctant to undergo reactions in which they must be converted to carbocations, undergo with ease reactions in which they must be carbanions and stable bridgehead carbanions are known."
Google has a habit of displaying cards, and I am sure several of you have seen these by now:
(search link)
The way I understand the purpose - of displaying cards for each answer (and not just the accepted answer) - is that it helps the viewer to get alternative ideas about the question, and t...
@GaurangTandon I'll be the first to congratulate you for being able to cast close votes \o/
Well, then it sounds like Usanovich, and also why his theory wasn't successful. Reasoning in vein of BiH3 barely holds to its protons and looses them in oxidation would be much better on your part. — Mithoron13 hours ago
@AvnishKabaj If possible , can you click pics of that topic and share it here ? I've searched it all over the internet , and I still am not sure what I'm doing when I solve the its problems.
Let's say you add $\ce{HCl}$ to water. The $\ce{H+}$ ion concentration increases and that causes a decrease in $\mathrm{pH}$. But why would the $\mathrm{pOH}$ increase?
I can't see why added $\ce{H+}$ ions will decrease the $\ce{OH}$ concentration? Is this because of the water auto-ionization? I...
This question is a follow up of another thread, where we are discussing Theresa May's accusation of the Russian government which is supposedly behind the recent chemical attack in Great Britain.
Soon, after the attack the Great Britain implemented a chemical analysis which again supposedly shows...
I think the barrier for 1,2 hydride shifts is usually fairly low, 10 kcal/m give or take. So I think A will try to equilibrate with B, and I think they likely have similar energies. In any case, as soon as any B is formed it will likely be siphoned off by a second 1,2 hydride shift to form a more stable tertiary carbocation.
Please reconsider your decision on voting buttons
The voting buttons are an ever-present aspect of a bunch of sites' graphical identity, and they pull a disproportionate amount of weight in making the theming feel like a complete skin rather than just some surface-level attributes. My main site ...
@ron that's very interesting, i never knew of the energies before; actually, the fact that you mentioned multiple subsequent shifts, reminds me of this question, which really deserves much better answers than it currently has
@EmilioPisanty Having a humble level of participation in at least more than one SE site, I can easily say that these vote buttons subconsciously remind me which site I am on, and give me a feeling of being "at home"
@ron yep, that's right. I mean, five of questions in the past month have a positive score but zero answers (a, b, c, d, e). I understand some of them may not have fuller answers, or some may require some level of abstraction (cont)
given a high schooler perspective; but I still think they deserve to be answered; but I don't know if this is the year of academia where all the grads/undergrads/profs are busy preparing their thesis or final year project, so several people may be busy around here