Then draw the resulting second resonance structure with lone pairs and charges. NOT YY 2 o& d) For both structures below begin by drawing the electron flow to generate a second resonance structure.
The following molecules according to the IUPCAC nomenclature system covered in ca ChemDraw as the format for naming will be different. # of 'H NMR signals = Splitting/Integration Table ex: H(x) = triplet (2H) # of C NMR signals total of alkane IC NMR signals of alkene aromatic HC NMR signals # of carbonyl SC NMR signals = #of 'H NMR signals = Splitting/Integration Table ex: H(x) = triplet (2H) # of SC NMR signals total = of alkans HC NMR signals # of alken/ aromatic 13C NMR signals = # of carbonyl 13C NMR signals = # of H NMR signals = Splitting Integration Table ex: H(x) = triplet (2H) #of IC NMR signals total #of alkans BC NMR signals - of alkenc/aromatic HC NMR signals # of carbonyl 13C NMR signals = In the table declare how many proton signals are expected and state the splitting and integration for each set of proton signals Use the structures on the right side of the page to complete the number of carbons total and the numbers of alkane alkene/aromatic and carbonyl carbons expected. Please enter your username or email address and your password to access the site. State Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware District of Columbia Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana. Draw the hydrogens on the structures on the left side of the page and label these protons as A.B.C.D. Sign in to register a product or access resources. College code in the United State or US territories.
For the three molecules, you will predict the proton and carbon NMR data by completing the given tables.
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