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Provide the correct IUPAC name for the skeletal (line-bond) structure shown here.
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- Plz do Asap...! With proper structures and explanation..!fill in the structure with any assumed c & h atoms. how do you know if or if not they belong there?Given is teh mass spectogram of an unknown compoound. This unstable cyclic compund is a colorless liquid with a sharp odor and reacts with light and air with long exposure. What is the molar mass of the target mecule? What is the Molecular formula of the target molecule? What IHD /U ? What could be the description of the structure? Give the name of the structure.
- Please help me with the organic chemistry question below. The solutions are linked, as it is one question with 2 parts: 1. A. Draw a molecular orbital diagram for (2E,4E)hexa-2,4-diene and ethene below. Make sure to label orbitals, HOMO, LUMO, nodes, antibonding/bonding, and fill correctly with electrons. 1. B. Use the orbitals drawn in the previous problem to determine if a cycloadditon would occur between the two compounds mentioned and if so, would it be suprafacial or antarafacial. Be sure to specify which orbitals you are using and use those orbitals to demonstrate your answer.5.) Which of the analine "units" in the Structure below would have the lowest pka which would have the highest A B H₂N. H₂N. O IZ NH₂ — с NH, D andpls help ASAP! “which term best describes the relationship between the following two molecules?”
- Propanal (bp 48°C) and propanol (bp 97°C), both found on Table 4.2, have very similar surfaceareas and dipole moments. Construct an explanation for the large difference in boiling pointsbetween the two.[32] which among NO2-, O3, and OF2 have delocalized pi electrons?What kind of isomerisation occur in the pairs a-f?
- For the Organic Chemistry topic of R and S, to make the structure R, does the prioritizing number have to be in order from 1 -> 2 -> 3 clockwise or can it be clockwise from 3 -> 2 -> 1?Analyze the CNMR and HNMR data attached in order to propose a structure with the molecular formula C8H8O2Most naturally occurring amino acids have chiral centers (the asymmetric a carbon atoms)that are named (S) by the Cahn–Ingold–Prelog convention (Section 5-3). The commonnaturally occurring form of cysteine has a chiral center that is named (R), however.(a) What is the relationship between (R)-cysteine and (S)-alanine? Do they have the oppositethree-dimensional configuration (as the names might suggest) or the same configuration?(b) (S)-Alanine is an l-amino acid (Figure 24-2). Is (R)-cysteine a d-amino acid or anl-amino acid?