Mohs’ scale of mineral hardness characterises the scratch resistance of various minerals through the ability of a harder material to scratch a softer. It was created by the German mineralogist Friedrich Mohs (1773-1839). Mohs based the scale on the ten readily available minerals.
Hardness | Mineral |
---|---|
1 | talc (Mg3Si4O10(OH)2) |
2 | gypsum (CaSO4·2H2O) |
3 | calcite (CaCO3) |
4 | fluorite (CaF2) |
5 | apatite (Ca5(PO4)3(OH-,Cl-,F-)) |
6 | orthoclase feldspar (KAlSi3O8) |
7 | quartz (SiO2) |
8 | topaz (Al2SiO4(OH-,F-)2) |
9 | corundum (Al2O2) |
10 | diamond (C) |
Mole (mol) is the SI base unit of amount of substance.
The mole is the amount of substance of a system which contains as many elementary entities as there are atoms in 0.012 kg of carbon 12.
When the mole is used, the elementary entities must be specified and may be atoms, molecules, ions, electrons, other particles, or specified groups of such particles. In this definition, it is understood that the carbon 12 atoms are unbound, at rest and in their ground state.
Minerals of the monoclinic crystal system are referred to three unequal axes. Two of these axes (a and c) are inclined toward each other at an oblique angle; these are usually depicted vertically. The third axis (b) is perpendicular to the other two and is called the ortho axis. The two vertical axes therefore do not intersect one another at right angles, although both are perpendicular to the horizontal axis.
a ≠ b ≠ c
α = γ = 90° ≠ β
Mustard agents are usually classified as blistering agents owing to the similarity of the wounds caused by these substances resembling burns and blisters. However, since mustard agents also cause severe damage to the eyes, respiratory system and internal organs, they should preferably be described as blistering and tissue-injuring agents. Normal mustard agent (yperite), 1,1-thio-bis-[2-chloroethane], reacts with a large number of biological molecules. The effect of mustard agent is delayed and the first symptoms do not occur between 2-24 hours after exposure. At room temperature, mustard agent is a liquid with low volatility and is very stable during storage.
Monosaccharides are carbohydrates, with the general formula Cn(H2O)n, that cannot be decomposed to a simpler carbohydrates by hydrolysis.
Depending on whether the molecule contains an aldehyde group (-CHO) or a ketone group (-CO-) monosaccharide can be a polyhydroxy aldehyde (aldose) or a polyhydroxy ketone (ketose). These aldehyde and ketone groups confer reduction properties on monosaccharides. They are also classified according to the number of carbon atoms they contain: trioses have three carbon atoms, tetroses four, pentoses five, hexoses six, heptoses seven, etc. These two systems of classification are often combined. For example, a six-carbon polyhydroxy aldehyde such as D-glucose is an aldohexose, whereas a six-carbon polyhydroxy ketone such as D-fructose is a ketohexose.
The notations D and L are used to describe the configurations of carbohydrates. In Fischer projections of monosaccharides, the carbonyl group is always placed on top (in the case of aldoses) or as close to the top as possible (in the case of ketoses). If the OH group attached to the bottom-most asymmetric carbon (the carbon that is second from the bottom) is on the right, then the compound is a D-sugar. If the OH group is on the left, then the compound is an L-sugar. Almost all sugars found in nature are D-sugars.
Monosaccharides can exist as either straight-chain or ring-shaped molecules. During the conversion from straight-chain form to cyclic form, the carbon atom containing the carbonyl oxygen, called the anomeric carbon, becomes a chiral center with two possible configurations (anomers), α and β. When the stereochemistry of the first carbon matches the stereochemistry of the last stereogenic center the sugar is the α-anomer when they are opposite the sugar is the β-anomer.
Mutarotation is the change in optical rotation accompanying epimerization. In carbohydrate chemistry this term usually refers to epimerization at the hemiacetal carbon atom. In general α- and β-form are stable solids, but in solution they rapidly equilibrate. For example, D-glucose exists in an equilibrium mixture of 36 % α-D-glucopyranose and 64 % β-D-glucopyranose, with only a tiny fraction in the open-chain form. The equilibration occurs via the ring opening of the cyclic sugar at the anomeric center with the acyclic form as the intermediate. Mutarotation was discovered by French chemist Augustin-Pierre Dubrunfaut (1797-1881) in 1846.
Nerve poison (nerve gas, agents) have had an entirely dominant role since the Second World War. Nerve poisons acquired their name because they affect the transmission of nerve impulses in the nervous system. All nerve poisons belong chemically to the group of organo-phosphorus compounds. They are stable and easily dispersed, highly toxic and have rapid effects both when absorbed through the skin and via respiration. Nerve poisons can be manufactured by means of fairly simple chemical techniques. The raw materials are inexpensive and generally readily available.
The most important nerve agents included in modern chemical weapons arsenals are:
Tabun | (o-ethyl dimethylamidophosphorylcyanide) |
Sarin | (isopropyl methylphosphonofluoridate) |
Soman | (pinacolyl methylphosphonofluoridate) |
GF | (cyclohexyl methylphosphonofluoridate) |
VX | (o-ethyl S-diisopropylaminomethyl methylphosphonothiolate) |
Nerve poisons are colorless, odorless, tasteless liquids of low volatility. Antidotes are atropine sulfate and pralidoxime iodide.
Newman’s projection is an image which we get when we observe a model of ethane molecule in C-C bond direction.
Nuclear reactor is an assembly of fissionable material (uranium-235 or plutonium-239) designed to produce a sustained and controllable chain reaction for the generation of electric power.
The essential components of a nuclear reactor are:
Generalic, Eni. "Curtain rod width." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
Glossary
Periodic Table