![]() ![]() ![]() The algebraic sum of the oxidation states in an ion is equal to the charge on the ion.Īssigning oxidation numbers to organic compounds.The algebraic sum of the oxidation numbers of elements in a compound is zero.Hydrogen has an oxidation number of +1 when combined with non-metals, but it has an oxidation number of -1 when combined with metals.Oxygen almost always has an oxidation number of -2, except in peroxides (H 2O 2) where it is -1 and in compounds with fluorine (OF 2) where it is +2.The alkaline earth metals (group II) are always assigned an oxidation number of +2.The alkali metals (group I) always have an oxidation number of +1.Fluorine in compounds is always assigned an oxidation number of -1.The oxidation number of a monatomic ion equals the charge of the ion.The oxidation number of a free element is always 0.You can find examples of usage on the Divide the redox reaction into two half-reactions page. Since the electrons between two carbon atoms are evenly spread, the R group does not change the oxidation number of the carbon atom it's attached to. Unlike radicals in organic molecules, R cannot be hydrogen. Organic compounds can be written in such a way that anything that doesn't change before the first C-C bond is replaced with the abbreviation R (Figure 1c). When dealing with organic compounds and formulas with multiple atoms of the same element, it's easier to work with molecular formulas and average oxidation numbers (Figure 1d). Notice that changing the CH 3 group with R does not change the oxidation number of the central atom. R is an abbreviation for any group in which a carbon atom is attached to the rest of the molecule by a C-C bond. Different ways of displaying oxidation numbers of ethanol and acetic acid. ![]()
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And even in the first case, sometimes you have odd line ending. ![]() This, in turn, makes the pages look ugly on the kindle, because either you resort to have (very) uneven/inconsistent spacing between a word and another, or maybe even worse, you accept having "left-alignment" on PW instead of justified text as you have in a printed page. Second, kfx formatting is just better: maybe you english readers don't notice it that much because you don't use it (but I might be very wrong on that), but absurdly enough, azw3 has no automatic hypenation! It has to be like "hardcoded" into the file - which in turn might be hard when you do searches I think - or you must resort to do without hypenation. And KFX advantages are not at all marginal to me.įor starters, KFX has ligatures, which azw3 doesn't have: kfx just look better on paperwhite, closer to a printed page. It's just that, at the end of the day, these are all instruments to let me do what I like the most, that is: reading. but it's fair, not arguing on what is best on that part. If I had any interest in that, I would just use epub and that's it. ![]() Not arguing to what is "closer to industry standard", I will just say that "close" is "close", from the ethical point of view. ![]() Then later many of us switched from reading on Kindle to reading on Kobo (including ebooks bought on Amazon). We stopped using Whispernet on bought books years ago (which was KFX) and instead used "Download and Transfer" which gives azw3 (except some old content is mobi/prc). Uploaders to Amazon don't create KFX, that uses docx or epub. Main advantages are being able to start reading during slow WiFi/Mobile download and for Amazon, more adaptive encryption. 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