greysteel_M6
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Posts posted by greysteel_M6
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your question is both confusing and annoying, how do you do it?
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no, get back with us in a few centuries
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google it, it's popular
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yes, the stability comes from the resonance of the pi orbitals, making in a sense a race track for electrons,
4=2n I do believe is the formula for electrons of rings that maintain this stability
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/\ the question isn't to draw out all possible variations, it points to predicting the relative stability, looking up stilbene there's 2 phynls that are attached at the benzylic position and double bonded, of course the trans isomer will be most stable
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Fluoroantimonic acid, the dissociation doesn't lie, -25.00!
Uh... strictly speaking, "acid" is actually a base.uh... once dissociated
it functions as an acid before it becomes the conjugate base
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well, amongst the garbage that's collecting in here, I'll explain
With respect to strong acids/bases, we have a species that has a great affinity to either take or give hydrogens away with respect to itself, a strong acid maintains a high affinity to donate its protons thus analogously it has a low affinity to give its protons away.
the graphs with a sharp curve and sudden change of pH correspond to
the analyte being consumed, therefore nothing is hindering the change of pH other than water
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How do molecules smell?
in Organic Chemistry
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ester = fruity smell
/\ are you serious? No we're in Iraq because we went in there to remove dangerous weapons from a dangerous regime, that prime objective failed and it has turned into some gd post-facto humanitarian mission.