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- Construct a simulated 1H NMR spectrum for 2-chloropropane by dragging and dropping the appropriate splitting patterns into the boxes on the chemical shift baseline, and by dragging integration values into the small box above each signal. Items may be used more than once. Peak heights do not represent integration. It has signals at 1.5 and about 3.8 ppmWhat is the order in which the H1 NMR singals would appear (from most downfield to most upfield) ? For each NMR signal expected, what is the integration value and multiplicity?THIS CAN NOT BE HAND-DRAWN! Interpret each of the following 1H NMR spectra. The integration for each peak is given above the peak. See the example for methyl ethyl ketone. All spectra were taken from http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi.
- PLEASE ASAP Compound C8H8O2 attached. What is a reasonable structure that is consistent with this data. Please explain in detail. Calculate theR value first! Each of the carbon signals is labeled to show how many H atoms are attached. Ignore the solvent signals at 78.5, 77.2, and 76.0 ppmFrom the spectra A-J and in the NMR Spectra tile, select the letter that corresponds to 1. methyl butanoate2. benzaldehyde3. 1-chlorobutane4. 1-chloro-2-methylpropane5. butan-2-one6. propan-2-ol7. propanalFully annotate proton nmr. Using specific pieces of data from the spectra please discuss how you determined the identity of the terpene unknown. Your answer should be 1-2 paragraphs.
- Create a table that summarizes: the chemical shift, integration, multiplicity, proton assignment, and justification of each signal based on the given spectrum. product is 4-ethylphenotole i believePlease assign all data in the spectra shown below. Set your peak assignments out in table format using the headings: 1H NMR, 13C NMR, Infrared spectrum and Mass spectrum Please find which 2 compounds are present in the spectra shown there are other 2 attachments which shows which compounds it could be?Consider the mass spectrum of hexan-2-amine. Label the molecular ion and base peak and propose a structure for the fragment that corresponds to the base peak.
- hi for organic compound below , can you please show the analyses of H NMR showing integration ppm splitting of peaks and functional group can you please also draw the different hydrogen environment on the compound structure please. naming as Ha , Hb etc i am confused with how to integrate the three peaks that are next to each otherORGANIC CHEMISTRY QUESTION Below is the mass spectrum for 1-(chloromethyl)-2-methylbenzene. The mass of the molecular ion is 140 m/z. Annotate the spectra with any and all relevant signals. This includes but is not limited to the base peak, molecular ion peak, key fragments, and other isotopic signals of relevance.Each annotation should be clearly marked and include the m/z.Using a 300 MHz NMR instrument: a.How many Hz downfield from TMS is a signal at 2.5 ppm? b. If a signal comes at 1200 Hz downfield from TMS, at what ppm does it occur? c.If two signals are separated by 2 ppm, how many Hz does this correspond to?