CARAVEL, or Carvel (from the Gr. κάραβος, a light ship, through the Ital. carabella and the Span. carabas), a name applied at different times and in different countries to ships of very varying appearance and build, as in Turkey to a ship of war, and in France to a small boat used in the herring fishery. In the 15th and 16th centuries, caravels were much used by the Portuguese and Spanish for long voyages. They were roundish ships, with a double tower at the stern, and a single one in the bows, and were galley rigged. Two out of the three vessels in which Columbus sailed on his voyage of discovery to America were “caravels.” Carvel, the older English form, is now used only in the term “carvel-built,” for a boat in which the planking is flush with the edges laid side to side, in distinction from “clinker-built,” where the edges overlap.
CARAVELLAS, a small seaport of southern Bahia, Brazil, on the Caravellas river a few miles above its mouth, which is dangerously obstructed by sandbars. Pop. (1890) of the municipality 5482, about one-half of whom lived in the town. Caravellas was once the centre of a flourishing whale fishery, but has since fallen into decay. It is the port of the Bahia & Minas railway, whose traffic is comparatively unimportant.
CARAWAY, the fruit, or so-called seed, of Carum Carui, an umbelliferous plant growing throughout the northern and central parts of Europe and Asia, and naturalized in waste places in England. The plant has finely-cut leaves and compound umbels of small white flowers. The fruits are laterally compressed and ovate, the mericarps (the two portions into which the ripe fruit splits) being subcylindrical, slightly arched, and marked with five distinct pale ridges. Caraways evolve a pleasant aromatic odour when bruised, and they have an agreeable spicy taste. They yield from 3 to 6% of a volatile oil, the chief constituent of which is cymene aldehyde. Cymene itself is present, having the formula CH3C6H4CH(CH3)2; also carvone C10H14O, and limonene, a terpene. The dose of the oil is ½-3 minims. The plant is cultivated in north and central Europe, and Morocco, as well as in the south of England, the produce of more northerly latitudes being richer in essential oil than that grown in southern regions. The essential oil is largely obtained by distillation for use in medicine as an aromatic stimulant and carminative, and as a flavouring material in cookery and in liqueurs for drinking. Caraways are, however, more extensively consumed entire in certain kinds of cheese, cakes and bread, and they form the basis of a popular article of confectionery known as caraway comfits.
CARBALLO, a town of north-western Spain, in the province of Corunna; on the right bank of the river Allones, 20 m. S.W. of the city of Corunna. Pop. (1900) 13,032. Carballo is the central market of a thriving agricultural district. At San Juan de Carballo, on the opposite bank of the Allones, there are hot sulphurous springs.
CARBAZOL, C12H9N, a chemical constituent of coal-tar and crude anthracene. From the latter it may be obtained by fusion with caustic potash when it is converted into carbazol-potassium, which can be easily separated by distilling off the anthracene. It may be prepared synthetically by passing the vapours of diphenylamine or aniline through a red-hot tube; by heating diorthodiaminodiphenyl with 25% sulphuric acid to 200° C. for 15 hours; by heating orthoaminodiphenyl with lime; or by heating thiodiphenylamine with copper powder. It is also obtained as a decomposition product of brucine or strychnine, when these alkaloids are distilled with zinc dust. It is easily soluble in the common organic solvents, and crystallizes in plates or tables melting at 238° C. It is a very stable compound, possessing feebly basic properties and characterized by its ready sublimation. It distils unchanged, even when the operation is carried out in the presence of zinc dust. On being heated with caustic potash in a current of carbonic acid, it gives carbazol carbonic acid C12H8N·COOH; melted with oxalic acid it gives carbazol blue. It dissolves in concentrated sulphuric acid to a clear yellow solution. The potassium salt reacts with the alkyl iodides to give N-substituted alkyl derivatives. It gives the pine-shaving reaction, in this respect resembling pyrrol (q.v.).