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.

Question: (a) Draw six (6) constitutional isomers of C6H12O2. Among your isomers, you must have at least one of the each of the following functional groups: alcohol, alkene, carboxylic acid, ether, ester and ketone. In addition, at least one of the isomers must contain a ring. Isomers may contain one or more of the listed functional groups.

The formula for this compound is C6H12O2. Solve the structure of this compound with only the ir and nmr spectra. The ir spectrum is obtained on a neat liquid sample.

A compound with the formula C6H12O2 has a mass spectrum and IR spectrum as describe-d below. By HNMR there are 2 sets of peaks, both singlets. What is the structure of this compound?

The proton NMR spectrum for a compound with the formula C6H12O2 is shown below along with carbon-13 spectral data in tabular form. (It may be necessary to expand (zoom) some of the 1H signals to view spin-spin splitting details.) This compound exhibits strong infrared absorption at 1738 and 1245 cm-1.

The structures of several isomeric esters, C6H12O2 (molar mass =116 ) are given below. A particular isomer does not produce an ion from a McLafferty rearrangement. This compound's base peak at m/z=43(M−73) results from an α-cleavage at the carbonyl group. A significant peak at m/z=57(M−59) is formed by an α cleavage in the alkoxy group.

Question: A compound with formula C6H12O2 has the IR and 1H NMR spectra as presented below. Draw the structure of this compound.

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).