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ACD/Labs Blog

Arvin Moser
Like a methoxy group, a t-Butyl group stands out over other 1H resonances. For organic compounds, the 1H resonance for a t-Butyl group generally towers over other 1H resonances because it integrates to ~9 protons (assuming the presence of 1 t-Butyl group and no overlap with other resonances). The basic 1H NMR pattern of the...

Arvin Moser
When trying to elucidate an unknown structure using 2D NMR information, an elucidator gains an advantage by analyzing all of the NMR data as a whole rather than as individual pieces. Although complicated at first, this different perspective at viewing the NMR data can facilitate the elucidation process. The following list are a few advantages...

Arvin Moser
MS and NMR are complementary tools for structure elucidation. Knowing when to apply which tool can assist an elucidator in solving for an unknown structure quickly and with less frustration. Although the sample data below is for a simple organic structure, it is working through many simple examples that one refines the skills needed for...

Arvin Moser
Although NMR offers some strategies for determining the presence of a fluorine atom(s), fragment loss of a CF3 group can be determined from a mass spectrum. The EI MS for 2,2,2-trifluoro-N,N-dimethylacetamide (Mmi = 141 Da) is shown below. The ion peak at m/z 72 indicates the loss of a CF3 group. Although the ion peak...

Arvin Moser
A 1H-1H COSY dataset of an unknown structure with protons offers many combinations of atom connectivity. The goal for the elucidator is to assess the correlations and narrow down a set of fragments that support the data. Below is a structural list for 1H to C to 1H connectivities. Absent from the list, heteroatoms such...

Arvin Moser
A component of structure elucidation involves the capability to interpret spectral data of an unknown compound. The interpretation of the data generally leads into a wide range of structural possibilities for the unknown. The goal of the elucidator is to narrow down the structural possibilities to a minimum set of fragments. Taking these fragments, the...

Arvin Moser
Without correctly identifying the molecular ion on a mass spectrum, the nitrogen rule generally cannot be applied to any arbitrary ion peak. The chemical structure for N-[(1E)-1-phenylethylidene]methanamine and its EI mass spectrum are shown below. As expected, the odd value for the molecular ion at m/z 133 dictates an odd number of nitrogen atoms. However,...

Arvin Moser
For MS data, the ionization method will dictate how the nitrogen rule is applied. For example, if the ionizer is Electron Impact (EI) ionization, then the nitrogen rule is to be applied to the molecular ion [M]+* as follows: -an odd nominal mass indicates an odd number of nitrogen atoms, e.g. 1,3,5 -an even nominal...

Arvin Moser
The purpose of the nitrogen rule is to assist with deciphering how many nitrogen atoms are present without any prior information on the molecular formula. Depending on the ionization mode, an odd nominal mass indicates an odd number of nitrogen atoms, e.g. 1,3,5, whereas an even nominal mass indicates an even number of nitrogen atoms,...