For example, the boiling points for n-pentane, isopentane, and neopentane at 1 atm are 36.1, 27.8, and 9.5 °C, respectively. Notice that n-pentane and isopentane both have much lower melting points than neopentane.
Pentane: Neopentane: Isopentane: This problem has been solved!
During recovery from anesthesia, those recovering form neopentane showed marked hyperexcitability when stimulated by noise or touch. See the answer. Each methyl group is considered a "branch". B. neopentane has a 3 carbon chain with two methyl groups on the 2nd carbon. Show transcribed image text.
Neopentane was less anesthetic and less lethal than isopentane, ... Neopentane differed from the others in causing still more excitement and a general cramp-like effect just before anesthesia was induced. C. Isopentane has a 4 carbon chain with 1 methyl group on the second carbon. Question: Rank These Compounds By Boiling Point. Expert Answer 100% (49 ratings) Step 2. The boiling point of alkane depends on their molecular mass and structure but boiling point of compounds having same molecular mass changes with their structure. Thus, neopentane's lower boiling point means that this isomer has a lower vapor pressure, which makes it is more likely to enter the atmosphere than the other two isomers under the same environmental conditions. This is because to assemble them into an ordered solid, all the flexible bonds in the chains in each molecule have to be twisted into the same shape, which is disfavoured by entropy (there's a higher penalty for imposing more order on a system). So we can rank them as Pentane, Isopentane, then neopentane. So all in all we have 0 methyl groups on A, 1 methyl group on C, and 2 methyl groups on B. Isopentane and neopentane are constitutional isomers of pentane, [math]\mathrm{C_5H_{12}}[/math].
Pentane, neopentane, and isopentane are isomers of each other.
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