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1. A .6M solution is made by dissolving compound X in water. After 10 secs the concentration of X is .4M. All of the following can account for this EXCEPT:
A Precipitation
B Neutralization
C Evaporation
D Decomposition
E Disproportionation
The answer is A, but i cant seem to reason it out..maybe b/c with ppt molarity??
2. And heres just an orgo question: Im under the impression that allylic carbocation is most stable followed by a tert. carbocation. Also, would three phenyl groups on a tert carbocation be more stable than 3 methyl groups..am i correct? Can someone please go through the whole stability thing b/w say phenyl vs methyl and allylic carbocation. Thanks in advance!
A Precipitation
B Neutralization
C Evaporation
D Decomposition
E Disproportionation
The answer is A, but i cant seem to reason it out..maybe b/c with ppt molarity??
2. And heres just an orgo question: Im under the impression that allylic carbocation is most stable followed by a tert. carbocation. Also, would three phenyl groups on a tert carbocation be more stable than 3 methyl groups..am i correct? Can someone please go through the whole stability thing b/w say phenyl vs methyl and allylic carbocation. Thanks in advance!
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