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- draw the strucutre based off the IR spectrum, 1H NMR spectrum, and 13C NMR spectrum for this compound. This compound is prepared from the anti-Markovnikov addition of water to phenylacetylene. Its molecular formula is C8H8O.Will the bonding of the Zn2+ ion to the ketone oxygen lone pair make theketone C=O easier or more difficult to reduce? Why?Answer the following question pertaining to the reaction of maleic anhydride and 1,3-butadiene: Why does 1,3-butadiene react more rapidly with maleic anhydride than with another molecule of itself?
- Provide the reagents necessary to carry out the conversion shown. 1. H2O; 2. KMnO4 1. O3; 2. DMS; 3. Na2Cr2O7/H2SO4/H2O 1. NaOH, Br2; 2. DMS; 3. H2O/heat 1. O3; 2. DMS; 3. KMnO4 1. DMS; 2. H2O2/heatdraw the strucutre based off the IR spectrum, 1H NMR spectrum, and 13C NMR spectrum for this compound. This compound is an ester that is commonly used as food additive to give foods and beverages a fruity flavor. Its molecular formula is C7H14O2How much cyclohexanone (MW=98.15, D=0.9478) will be formed with 100% conversion of cyclohexanol (MW=100.158, D=0.9624)?
- What spectral features including mass spectra, IR spectra, proton spectra and carbon spectra allow you to differentiate the product (Benzonitrile) from the starting material (Benzoic Acid)? Show IR,MS,HNMR,CNMR seperatlyAfter E2 elimination, will the following molecule contain deuterium? Why or why not?Please help. Questions in images. Solvent Rf of A Rf of B Rf of C 10% ethyl acetate-90% hexanes .12 .07 .01 20% ethyl acetate-80% hexanes .34 .29 .10 30% ethyl acetate-70% hexanes .53 .42 .22 40% ethyl acetate-60% hexanes .72 .61 .35
- Consider the product below a) Would this product show a signal in a UV-Vis spectrum? Why? b) Would this molecule have a non-zero alpha-value in polarimetry? Why? c) What stretches would be expected in an IR spectrum of this molecule? d) Predict the 1H NMR spectrum for this molecule. For H1 to H6 e) Predict the 13C NMR spectrum and DEPT spectra for Carbon A- Carbon G. Use (+) for positive signals, (-) for negative signals, and (X) for no signal in the DEPT NMR spectra. f) If a base such as NaOH was used, it would be harder to determine the major product before running the reaction. Once the reaction was run, how would you determine the product favored using spectroscopy?Compound A is first reacted with methylamine in the presence of acid and then treated with NaBH3CN. Using the spectroscopic data given, what is the structure of the product after step 1?1. In both SN1 and SN2 tests, why should 2-chlorobutane react more slowly than 2-bromobutane?2. Why is benzyl chloride reactive in SN1? In SN2?3. Why is bromobenzene unreactive in both tests?