A compound has the molecular formula. C6H12O2. Its IR spectrum shows a strong absorption band near 1740 cm-1 ; its 1H NMR spectrum consists of two singlets, at delta 1.4 and delta 2.0. The most likely structure for this compound is:

Question: 1. Choose the reaction that represents the combustion of C6H1202. A) C6H12O2(1) + 8 O2(g) →6 CO2(g) + 6H2O(g) B) Mg(s) + C6H12O2(1) - MgC6H12O2(aq) C) 6 C(s) + 6 H2(g) + O2(g) → C6H12O2(1) D) C6H12O2(1)→ 6 C(s) + 6 H2(g) + O2(g) E) None of the above represent the combustion of C6H1202 2.

Provide a structure for the following compound: C6H12O2: IR: 1743 cm-1; 1H NMR spectrum: Your solution’s ready to go! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

The 1H-NMR of a compound with molecular formula C6H12O2 consists of four signals: 1.1 (triplet, integrating to 3 Hydrogens), 1.2 (doublet, integrating to 6 Hydrogens), 2.3 (quartet, integrating to 2 Hydrogens) and 5.0 (septet, integrating to 1 Hydrogen). Propose a structural formula for this compound consistent with this information.

C6H12O2; IR: 1743 cm−1; 1H NMR spectrum Your solution’s ready to go! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

Answer to Problem 1: C6H12O2 Analysis of infrared spectrum & 300 MHz 'H NMR In CDC13 3H, J = 6.8 Hz 3H, J = 7.2 Hz 2H, J = 6.8 Hz 2H, J = 7.2 Hz 2H, J = 7.2 Hz 5 4 3 N 1 0 2 resonances 200 180 160 140 120 100 80 60 40 20 0 FTIR NEAT 100 Прум 90 80 70 60 2939.0 20090 % Transmittance 1303.6 1371.1 1255.4 1027.9 1095.4 50 2967.9 40 30 1186.0 20 1739.5 10 4500 4250 4000 3750 3500 3250 3000 ...

Compound A, C6H12O2, was found to be optically active and was slowly oxidized to an optically active carboxylic acid B, C6H12O3, by Tollen’s Reagent [Ag(NH3)2+] {The “Silver Mirror” Test}. Oxidation of A by anhydrous CrO3 gave an optically inactive compound that reacted with Zn amalgam/HCl [Clemmensen Reduction] to give 3-Methylpentane.

Draw the structure of a compound that fits the description: An ester of molecular formula C6H12O2 that contains a methoxy group (OCH3) bonded to the carbonyl group. Your solution’s ready to go! Our expert help has broken down your problem into …

Question: The 1H- and 13C-NMR spectra for an unknown compound with molecular formula C6H12O2 are shown below. Deduce a structural formula for this compound. The 1 H- and 13 C-NMR spectra for an unknown compound with molecular formula C 6 H 12 O 2 are shown below.

5 (20 Points). Spectroscopy. a (10 Points). An unknown compound has a molecular formula of C6H12O2. It's IR spectrum has a band at 1745 cm and the 'H NMR spectrum is shown below. Provide a structure for this compound. Partial credit maybe awarded if you show your work. بالایی 2.1 2.0 1.9 ppm 4.0 کد 3.0 2. 2.0 کو1 1.0 ppm b (10 Points).