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one place is midnight at the other, the longest day corresponds to the shortest, and mid-winter is contemporaneous with midsummer. In the calculation of days and nights, midnight on the one side may be regarded as corresponding to the noon either of the _previous_ or of the _following_ day. If a voyager sail eastward, and thus anticipate the sun, his dating will be twelve hours in advance, while the reckoning of another who has been sailing westward will be as much in arrear. There will thus be a difference of twenty-four hours between the two when they meet. To avoid the confusion of dates which would thus arise, it is necessary to determine a meridian at which dates should be brought into agreement, i.e. a line the crossing of which would involve the changing of the name of the day either forwards, when proceeding westwards, or backwards, when proceeding eastwards. Mariners have generally adopted the meridian 180 deg. from Greenwich, situated in the Pacific Ocean, as a convenient line for co-ordinating dates. The so-called "International Date Line," which is, however, practically only due to American initiative, is designed to remove certain objections to the meridian of 180 deg. W., the most important of which is that groups of islands lying about this meridian differ in date by a day although only a few miles apart. Several forms have been suggested; these generally agree in retaining the meridian of 180 deg. in the mid Pacific, with a bend in the north in order to make the Aleutian Islands and Alaska of the same time as America, and also in the south so as to bring certain of the South Sea islands into line with Australia and New Zealand. ANTIPYRINE (phenyldimethyl pyrazolone) (C11H12N2O), is prepared by the condensation of phenylhydrazine with aceto-acetic ester, the resulting phenyl methyl pyrazolone being heated with methyl iodide and methyl alcohol to 100-110 deg. C.: CH3.C=N \ CH3.C-N.CH3 >N.C6H5 -> || >N.C6H5 CH2-CO / HC-CO Phenyl methyl pyrazolone Antipyrine On the large scale phenylhydrazine is dissolved in dilute sulphuric acid, the solution warmed to about 40 deg. C. and the aceto-acetic ester added. When the reaction is complete the acid is neutralized with soda, and the phenyl methyl pyrazolone extracted with ether and distilled _in vacuo_. The portion distilling at about 200 deg. C. is then methylated by means
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