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2. Neopentane - Wikipedia

   en.wikipedia.org/wiki/Neopentane

   Therefore, neopentane is a gas at room temperature and atmospheric pressure, while the other two isomers are (barely) liquids. The melting point of neopentane (−16.6 °C), on the other hand, is 140 degrees higher than that of isopentane (−159.9 °C) and 110 degrees higher than that of n -pentane (−129.8 °C).

3. 2,2-Dimethylbutane - Wikipedia

   en.wikipedia.org/wiki/2,2-Dimethylbutane

   Butlerov's student V. Goryainov originally discovered neohexane in 1872 by cross-coupling of zinc ethyl with tert-butyl iodide. [5]2,2-Dimethylbutane can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.

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5. Neopentyl alcohol - Wikipedia

   en.wikipedia.org/wiki/Neopentyl_alcohol

   Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride.

6. n-Butylbenzene - Wikipedia

   en.wikipedia.org/wiki/N-Butylbenzene

   n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9.Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group.

7. 1-Bromopentane - Wikipedia

   en.wikipedia.org/wiki/1-Bromopentane

   Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] It is also formed by the reaction of 1-pentanol with hydrogen bromide.

8. Nickelocene - Wikipedia

   en.wikipedia.org/wiki/Nickelocene

   Nickelocene was first prepared by E. O. Fischer in 1953, shortly after the discovery of ferrocene, the first metallocene compound to be discovered. [4] It has been prepared in a one-pot reaction, by deprotonating cyclopentadiene with ethylmagnesium bromide, and adding anhydrous nickel(II) acetylacetonate. [5]

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