PRINCIPLES OF MODERN CHEMISTRY-OWLV2
8th Edition
ISBN: 9781305271609
Author: OXTOBY
Publisher: CENGAGE L
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- An unknown has a molecular ion with a mass of 134. The relative abundance of the peak at 135 is 9.9%what is the molecular formula of the unknown how many rings or pi binds is the unknown propose 2 structures for the unknown how could you distinguish your answers to "c" using 13 C NMRarrow_forwardPlease correct answer and don't used hand raiting and don't used Ai solutionarrow_forwardPractice: Draw all possible products using the reagents on the previous page 1+ DH H₂O* HBr, ROOR 1) Hg(OAc)2. H₂O 2) NaBH HR HX 1) O 2) DMS 1) OsO 1) BH, ⚫ THF 2) H₂O₂, NaOH PL H₁₂O⭑ HBr. ROOR 1) Hg(OAc)2. H₂O 2) NaBH4 1) BH₁ - THF 2) H₂O₂, NaOH Brz 2) NaHSO H₂O KMnO4 NaOH, cold 1) RCO₂H 2) H₂O* Br₂, H₂O na 1) O 1) OsO 2) DMS bro HX 2) NaHSO H₂O KMnO4 fa Bra NaOH, cold 1) RCO₂H 2) H₂O* Br₂, H₂O 11.5 notarrow_forward
- Please correct answer and don't used hand raitingarrow_forwardIdentify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic. H HAarrow_forwardConsider the titration of 100 mL of 0.100 M NaCl solution w/ 0.100 M AgNO3. Ecell after addition of 50 mL. Ecell after addition of 75 mL. Ecell after addition of 100 mL (equivalence point). Ecell after addition of 105 mL.arrow_forward
- Cyclohexene and 2 hexyne both have the molecular formula C6H10. How would you use infrared spectroscopy to distinguish between these two compounds?arrow_forwardPlease correct answer and don't used hand raitingarrow_forwardHow could you distinguish between the following isomers by 13C-NMR: a. 1,2-Dimethylbenzene b. 1,3-Dimethylbenzene C. 1,4-Dimethylbenzene.arrow_forward
- Per mole of fast, af males of C-C CH C-O OR bonda beads bonds- bonds Bond energy (kJ/mol) broken broken broken formed bonds formed methane 4 345 O 0 C-H 415 C-O 741 propane 2 8 5 0 0 0-11 464 00 498 hexane 5 17 14 19/20 18 25 25 160 14 All (kJ/mol fact) moles CO, produced (koel) per mole of fuel methane-82 propane -42.4 -31.1 hexane octanearrow_forwardPredict the splitting patterns you would expect for each proton in the molecules below. c. doublet a. septet H CH3 b. singlet d. quartet C1 Harrow_forwardWhich structure of molecular formula C4H8C12 fits both the 'H NMR and 13C NMR spectra shown + Cl A. B. Cl C. a D. Cl 10 00-228 Low? 9 8 7 6 5 ppm 'H NMR 40 40 -89 200 180 160 140 120 100 -8 80 60 13 3 2 1 0 CD8-03-793 ppm 13C NMR 20 -20 0 An unknown has a molecular ion with a mass of 134. The relative abundance of the peak at 135 is 9.9%. a. What is the molecular formula of the unknown? b. How many rings or pi-bonds in the unknown? c. Propose two structures for the unknown. d. How could you distinguish your answers to "c" using 13C-NMR? Identify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic. H HAarrow_forward
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