The identity of a carbonyl-containing compound has been narrowed down to three possibilities: acetamide (ethanamide), acetone (propanone), or 1,1,1-trichloropropanone. 1H NMR and IR spectral data for the compound are given below. Determine the structure, and thus the identity, of the compound that gives the observed data.

a. acetone
b. tricolorpropnone
c. acetamide

Lem 2 the data below are for the system ethyl propyl ether (1)-chloroform (2) at 0.5 bar. use the data to answer the following questions (all questions refer to p d 0: 5 bar). a) what are the boiling points of the pure components at 0.5 bar? b) a mixture with the overall composition z1 d 0: 1 is brought to 47.6ä±c, 0.5 bar. what is the phase? c) 100 mole of a mixture with z1 d 0: 1 (state a) is mixed with 22 mole of pure ethyl propyl ether vapor (state b). the mixing takes place at 47.6 ä±c, 0.5. bar. what is the phase of the resulting mixture (state c)? if the state is a v/l mixture report the number of moles and mole fractions in each phase. d) plot the txy graph and show states a, b and c. the graph must be done by computer and should be properly annotated. ethyl propyl ether (1) - chloroform (2) at 0.5 bar t ( ä±c) x1 y1 t ( ä±c) x1 y1 42.9 0.000 0.000 49.0 0.470 0.455 43.0 0.020 0.010 49.1 0.520 0.520 43.9 0.065 0.029 48.9 0.567 0.592 45.4 0.156 0.089 48.3 0.652 0.720 46.4 0.215 0.142 47.6 0.745 0.815 47.6 0.296 0.223 46.7 0.822 0.872 48.3 0.362 0.302 45.7 0.907 0.937 48.7 0.410 0.375 44.6 1.000

For each of the following compounds, decide whether the compound's solubility in aqueous solution changes with ph. if the solubility does change, pick the ph at which you'd expect the highest solubility. you'll find ksp data in the aleks data tab. compounds does solubility change with ph

As changes in energy levels of electrons increase, the frequencies of atomic line spectra they emit