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To get a IUPAC name for a certain molecule you just draw the molecule, select that molecule and click Tools and then click Generate Name. You can easily draw and use whole periodic table within the vertical tool bar. You can draw double and triple bond just by double/triple click on the single bond.
The principal characteristic groups here are obviously the aldehydes. Notably, P-33.1 states that "only one [suffix] can be placed at the end of a name to indicate the principal characteristic group", so the alcohol is now relegated to being a prefix, i.e. "hydroxy-". The next step is to decide on the "parent structure": P-44.1.1
During my studies of heterocyclic compounds I learned that monocyclic compounds has prefix+ stem+ suffix. the prefix is coming from the heteromolecule name (e.g oxgen --> oxa- ) however the stem and suffix is ambiguous to me. I can link some of the stem (e.g et --> from tETra) but what about all other stems and suffixes. Where do they came from?
For example, a preferred IUPAC name is 3-bromocyclohex-1-ene (not 1-bromocyclohex-2-ene): (This example is given in the Blue Book.) P-14.3.5 Lowest set of locants The lowest set of locants is defined as the set that, when compared term by term with other locant sets, each cited in order of increasing value, has the lowest term at the first ...
The IUPAC name for this compound would be 3[ 1' - bromomethyl] - hexane //Edit: Where 1' refers to the carbon in the methyl group attached to the 3rd carbon in the primary chain. Also if you had an ethyl group attached and if the Bromine was attached to the 1st or 2nd carbon in that chain then it would be 1' -bromoethyl....
For carbohydrates such as glucose, the current IUPAC recommendations do not identify a PIN. The systematic name for the β-pyranose form of ᴅ-glucose is (2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol. Since this name may be too cumbersome, a semisystematic name may be formed based on the retained name ᴅ-glucose as ...
The IUPAC Blue Book defines rules where locants can be ommitted in IUPAC preferred names. Unlike terminal locants in names for aldehydes that are omitted, there is no rule for homogeneous chains with three or more identical atoms that would allow for the ommission of the locant $2$ in propan-2-one.
If the name is correct. Then we can logically build up the resulting salt from the name. Let’s start with the cation: It is platinum(II), so we get $\ce{Pt^2+}$ adding four ammine ligands gives us $\ce{[Pt(NH3)4]^2+}$ For the anion: It is still platinum(II) (although rendered as platinate, so we need to end up with an anion): $\ce{Pt^2+}$
For example, to name the silicon analogue of thiophene either $1H$-Silole, or Sila-2,4-cyclopentadiene. Don't overly rely on these programs, though. If you read the rules and literature, for example, you will find out that 1H-pyrrole is possible , but in cases without ambiguity called pyrrole only.
What is the iupac name for ch3ch2cooag? [closed] Ask Question Asked 6 years, 9 months ago.