Physical property periodic table

Trends like those noted with the alkali metals are also seen with the alkaline earths. Reactivity again increases as you go down the column in the periodic table. Physical property trends are less evident among the alkaline earths. 

It should be noted that there is not always this consistency in property variations withm the periodic table. Physical properties change in a more or less regular manner however, there are some rather abrupt changes when one moves across a period or down a group. 

An account of the periodic law was given in 1876 by H. E. Armstrong and from about 1884 appeared in several English text-books. Thomas Carnelley extended the periodicity of physical properties to compounds. Wyrouboff, who did important research on isomorphism, said Mendeleeff s selection of the typical oxides (see top of table on p. 896) is arbitrary sometimes the lower oxide is selected (CugO), sometimes the higher (Mn207). 

Moseley s discovery was consistent with Mendeleev s ordering of the periodic table by properties rather than strictly by atomic mass. Eor example, according to Moseley, tellurium, with an atomic number of 52, belongs before iodine, which has an atomic number of 53. Today, Mendeleev s principle of chemical periodicity is correctly stated in what is known as the periodic law The physical and chemical properties of the elements are periodic functions of their atomic numbers. In other words, when the elements are arranged in order of increasing atomic number, elements with similar properties appear at regular intervals. 

The elements in the periodic table are arranged by atomic number. The elements are arranged in horizontal rows called periods and vertical columns called groups. The physical and chemical properties of an element can be estimated from its position in the periodic table. Two properties that help us explain the properties of organic compounds are the atomic radius and electronegativity. 

The trends in chemical and physical properties of the elements described beautifully in the periodic table and the ability of early spectroscopists to fit atomic line spectra by simple mathematical formulas and to interpret atomic electronic states in terms of empirical quantum numbers provide compelling evidence that some relatively simple framework must exist for understanding the electronic structures of all atoms. The great predictive power of the concept of atomic valence further suggests that molecular electronic structure should be understandable in terms of those of the constituent atoms. 

The development of the structural theory of the atom was the result of advances made by physics. In the 1920s, the physical chemist Langmuir (Nobel Prize in chemistry 1932) wrote, The problem of the structure of atoms has been attacked mainly by physicists who have given little consideration to the chemical properties which must be explained by a theory of atomic structure. The vast store of knowledge of chemical properties and relationship, such as summarized by the Periodic Table, should serve as a better foundation for a theory of atomic structure than the relativity meager experimental data along purely physical lines. ... 

Properties. Anhydrous potassium fluoride [7789-23-3] is a white hygroscopic salt that forms two hydrates, KF -2H20 [13455-21-5] and KF 4H2O [34341 -58-7]. The tetrahydrate exists at temperatures below 17.7°C. The dihydrate is stable at room temperature and starts to lose water above 40°C. Temperatures on the order of 250—300°C are requited to remove the last few percent of water ia a reasonable period of time. Potassium fluoride does not pyrohydroly2e at temperatures as high as 1000°C (1). Chemical and physical properties of KF are summarized ia Table 1. 

Physical Properties. Molybdenum has many unique properties, leading to its importance as a refractory metal (see Refractories). Molybdenum, atomic no. 42, is in Group 6 (VIB) of the Periodic Table between chromium and tungsten vertically and niobium and technetium horizontally. It has a silvery gray appearance. The most stable valence states are +6, +4, and 0 lower, less stable valence states are +5, +3, and +2. 

Nickel occurs in the first transition row in Group 10 (VIIIB) of the Periodic Table. Some physical properties are given in Table 1 (1 4). Nickel is a high melting point element having a ductile crystal stmcture. Its chemical properties allow it to be combined with other elements to form many alloys. 

Rubidium [7440-17-7] Rb, is an alkali metal, ie, ia Group 1 (lA) of the Periodic Table. Its chemical and physical properties generally He between those of potassium (qv) and cesium (see Cesiumand cesium compounds Potassium compounds). Rubidium is the sixteenth most prevalent element ia the earth s cmst (1). Despite its abundance, it is usually widely dispersed and not found as a principal constituent ia any mineral. Rather it is usually associated with cesium. Most mbidium is obtained from lepidoHte [1317-64-2] an ore containing 2—4% mbidium oxide [18088-11-4]. LepidoHte is found ia Zimbabwe and at Bernic Lake, Canada. 

Barium is a member of the aLkaline-earth group of elements in Group 2 (IIA) of the period table. Calcium [7440-70-2], Ca, strontium [7440-24-6], Sr, and barium form a closely aUied series in which the chemical and physical properties of the elements and thek compounds vary systematically with increa sing size, the ionic and electropositive nature being greatest for barium (see Calcium AND CALCIUM ALLOYS Calcium compounds Strontium and STRONTIUM compounds). As size increases, hydration tendencies of the crystalline salts increase solubiUties of sulfates, nitrates, chlorides, etc, decrease (except duorides) solubiUties of haUdes in ethanol decrease thermal stabiUties of carbonates, nitrates, and peroxides increase and the rates of reaction of the metals with hydrogen increase. 

A number of subdivisions of the maceral groups have been developed and documented by the International Commission on Coal Petrology (14). Table 1 Usts the Stopes-Heeden classification of higher rank coals. Periodic revisions include descriptions of the macerals, submacerals, morphology, physical properties, and chemical characteristics. Theories on the mode of formation of the macerals and their significance in commercial appUcations are also included of Reference 14. 

Among the alkali metals, Li, Na, K, Rb, and Cs and their alloys have been used as exohedral dopants for Cgo [25, 26], with one electron typically transferred per alkali metal dopant. Although the metal atom diffusion rates appear to be considerably lower, some success has also been achieved with the intercalation of alkaline earth dopants, such as Ca, Sr, and Ba [27, 28, 29], where two electrons per metal atom M are transferred to the Cgo molecules for low concentrations of metal atoms, and less than two electrons per alkaline earth ion for high metal atom concentrations. Since the alkaline earth ions are smaller than the corresponding alkali metals in the same row of the periodic table, the crystal structures formed with alkaline earth doping are often different from those for the alkali metal dopants. Except for the alkali metal and alkaline earth intercalation compounds, few intercalation compounds have been investigated for their physical properties. 

In so far as the chemical (and physical) properties of an element derive from its electronic configuration, and especially the configuration of its least tightly bound electrons, it follows that chemical periodicity and the form of the periodic table can be elegantly interpreted in terms of electronic structure. 

Periodic function A physical or chemical property of elements that varies periodically with atomic number, 152 Periodic Table An arrangement of the elements in rows and columns according to atomic numbers such that elements with similar chemical properties foil in the same column,... 

Thermal equilibrium, 56 Thermite reaction, 122 Thermometers, 56 Thiosulfate ion, 362 Third-row elements, 101 compounds, 102 physical properties, 102 properties, table, 101 Third row of the periodic table, 364 Thomson, J. J., 244 Thomson model of atom, 244 Thorium... 

In an article that first appeared in the Journal of Chemical Education, I considered the relationship, or perhaps the tension, between the periodic table of the elements arranged according to chemical properties and the periodic table of the atoms coming largely from the field of physics. This is a subject that continues to be at the center of my interests, although I have changed my mind on a number of issues as these papers will show. 

The use of the older restricted version of the Pauli principle has persisted, however, and is routinely employed to develop the electronic version of the periodic table. Modern chemistry appears to be committing two mistakes. Firstly, there is a rejection of the classical chemical heritage whereby the classification of elements is based on the accumulation of data on the properties and reactions of elements. Secondly, modem chemistry looks to physics with reverence and the false assumption that therein lies the underlying explanation to all of chemistry. Chemistry in common with all other branches of science appears to have succumbed to the prevailing tendency that attempts to reduce everything to physics (11). In the case of the Pauli principle, chemists frequently fall short of a full understanding of the subject matter, and... 

The closet precursor to Mendeleev s table in both chronological and philosophical toms was developed by Julius Lothar Meyer, a German chemist, in 1864. Although Meyer stressed physical rather than chemical properties, his table bears remarkable similarity to the one that Mendeleev would develop five years later. For a number of reasons, Meyer s prominence in tlte history books never matched Mendeleev s. There was an untimely delay in the publication of his most elaborate periodic table, and, perliaps more important, Meyer—unlike Mendeleev—hesitated to make predictions about unknown elements. 

Suffice it to say that Dobereiner s research established the notion of triads as a powerful concept, which several other chemists were soon to take up with much effect. Indeed, Do-bereiner s triads, which would appear on the periodic table grouped in vertical columns, represented the first step in fitting the elements into a system that would account for their chemical properties and would reveal their physical relationships. 

The chemistry of plutonium is unique in the periodic table. This theme is exemplified throughout much of the research work that is described in this volume. Many of the properties of plutonium cannot be estimated accurately based on experiments with lighter elements, such as uranium and neptunium. Because massive amounts of plutonium have been and are being produced throughout the world, the need to define precisely its chemical and physical properties and to predict its chemical behavior under widely varying conditions will persist. In addition to these needs, there is an intrinsic fundamental interest in an element with so many unusual properties and with so many different oxidation states, each with its own chemistry. 

The periodic table is one of the most notable achievements in chemistry because it helps to organize what would otherwise be a bewildering array of properties of the elements. However, the fact that its structure corresponds to the electronic structure of atoms was unknown to its discoverers. The periodic table was developed solely from a consideration of physical and chemical properties of the elements. 

As in the discussion of hydrogen, in this section we examine the properties of the alkali metals in the context of the periodic table and focus on significant applications of the elements and selected compounds. The valence electron configuration of the alkali metals is s1, where n is the period number. Their physical and chemical properties are dominated by the ease with which the single valence electron can be removed (Table 14.3). 

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