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Please provide the unknown structure for the NMR given
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- Chemistry Calculate the degree of unsaturation in the following formulas. C7H10Cl2 C17H23NO3 (Atropine) Draw the organic product of the following reaction.which of the following cannot be distinguished by an infrared spectrum a) resonant hybrids b) tautomers (keto-enol) c) enantiomers d) cis-trans isomersCr2(CH3COO)4(H2O)2 was prepared using the following reaction: 2Cr3+ + Zn(s) --> 2Cr2+ + Zn2+ 2Cr2+ + 4CH3COO- + 2H2O --> Cr2(CH3COO)4(H2O)2 (s) Discuss this reaction and how the reagents react with one another to form the product.
- How many isomeric dimethylcyclobutanes are thereThe 3 compounds below may be distinguished by simple chemical tests. CH3CH2COCH3. CH3CH2OH CH3CH3HO. Describe chemical tests that you could carry out to identify each Compound. State reagents used, essential conditions and expected observationsDraw the structural formula for at least one bromoalkene with the molecular formula C5H9Br that shows: Q.Both chirality and E,Z isomerism
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- Determine the degree of unsaturation and then draw possible structures for noncyclic compounds with the following molecular formulas: a. C3H6 b. C3H4 c. C4H6What is the degree of unsaturation and structure for C8H5NO2 ?Propose a structure for the compound that fits the following description. C10H14 7.18 δ, (4H, broad singlet) 2.70 δ (4H, quartet J = 7 Hz) 1.20 δ (6H. triplet J = 7 Hz) IR: 745 cm-1 7(a) IR absorption indicate the compound is .........-disubstituted = 7(b) The name of the compound is =