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- Identify the pro-R and pro-S groups/atoms in the following molecule, justifying your answer.predict the structure of the unknown compound using the image attached. Annotate all spectraEach spectra must be used to arrive at the answerThis means each piece of provided information should be annotated in some way depending on the type of analysis and information gained from it.calculate the HDI for proposed structure and provide the chemical formulaprovide the strcture of a compond that is consistent with the following IR and MS data: NOTE the mass of the molecular ion is 102.
- Which of the following statements about the molecule below are FALSE? Briefly explain your answer.1. When the following compound is subjected to mass spectrometry, which of the indicated bond(s) is (are) likely to cleave? Select all that apply.d. Supply a molecular formula and a possible structure for the compound shown here. explain please and show the calculations
- Benzene (electronic structure, hybridization, bond angles, geometry, complete structureshowing all atoms and bonds, resonance structures, and names of benzene derivatives. clear and short answer pleaseMake a continuous model for C4H10 by using 4 black 4 hole carbon atoms, 10 white one hole hydrogen atoms, and 13 pink bonds. Then write in wedge dash notation C4H10 and add in missing hydrogen atoms.pls help ASAP! “which term best describes the relationship between the following two molecules?”
- Compound C6H10O has the infrared spectrum shown below. Draw areasonable structure that is consistent with this data. Please explain work. Calculate the Rvalue first! -This compound has two common functional groups.What molecule does this IR sprectrum show? Please explain how you got this answer. Thank You!Please help answering the all parts of the following question...thank a.) Given that the condensed molecular formula for the following compound, C5H12O, predict the bonds you would expect this molecule to have based on the given IR spectrum. Draw arrows to the peaks with the bond(s) they represent. b.) Based on your findings from the IR spectrum, propose 3 different constitutional isomers that are consistent with your findings.