Can you please explain to me how I can better identify the IMF in organic chemistry? I have trouble looking at the molecules and being able to tell what forces are at play.
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Can you please explain to me how I can better identify the IMF in
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- Please don't provide handwritten solution ....For the following descriptions of molecules, draw the Lewis structure (showing all atoms, lone pairs, formal charges) of the molecule and show all bond angles (assuming ideal VSEPR angles). An organic compound with the molecular formula H3CNO2. C is sp2 hybridized, N is sp3 hybridized, one O is sp² hybridized, while the second O is sp3 hybridized. An organic compound with the molecular formula H2CNO*. Both C and O are sp hybridized while N is sp³ hybridized.Use the following set of assumptions to estimate the CN bond length in fulminic acid: 1) only the two best structures contribute to the true structure 2) the best structure contributes 75%, 3) the CN single bond is 1.47 pm, the double is 1.32 pm and the triple is L.16 pm. Enter your answer with 2 significant figures as a number with no units. Structure I Structure II Structure III H-C=N=0 H-C=N-0 ŌI H-C-N=01 VFullsc 10:41 PM
- The below picture is the electrostatic potential plot for valine molecule. The blue regions are areas of positive charge, the red regions are areas of negative charge, and the clear regions are areas of neutral charge. Comment on the charge distribution of valine and whether this makes sense based on the polarity of the bonds in the molecule. Additonally, explain there is negative charge for oxygen and positive charge for carbonUse VSEPR theory to predict the shape of this molecule (POC13) and indicate any deviation from the bond angle(s) expected from a regular arrangement of repulsion axes. Show all the steps took to arrive at answer 4 to five sentencesBriefly explain why the aromatic hydrocarbon azulene, C10H8, possesses a significant dipole moment. Use diagrams as needed to illustrate/clarify your answer.
- 2. It has been reported that 3-electron bonds may be possible. These bonds would be similar to "normal" two-electron bonds, except that three electrons would be required for each bond. I was curious as to what might happen to molecular geometries if ALL bonds involved three electrons and ALL lone pairs were actually lone triplets. Under this system, and using the VSETR (Valence Shell Electron Triplet Repulsion) Model, predict the ideal molecular geometries of the following molecules. (NOTES: The number of valence electrons for each atom remains the same; only worry about VSE Triplets around the central atom; electron triplets would still want to position themselves around the atom just like doublets.) a. FH;2 b. ХеН c. FH2 d. H30thx!Give a clear handwritten answer with explanation
- 2. In measurements of the structure of molecules, some interesting trends are observed. The bond angle (H-C-H) in CH4 is 109°, as we would expect for a molecule in the tetrahedral VSEPR class. However, other molecules in the same VSEPR class, such as ammonia (NH3, H-N-H= 107°) and water (H2O, H-O-H = 105°), have smaller bond angles than expected. Explain the basis for the bond angle trend: CH4 > NH3 > H2O. %3DCompare these two structures. [0=C=N] [0=C—N: Determine whether the two represent resonance contributors of a single species or depict different substances. If two structures are not resonance contributors, explain why. Select the single best answer. O The two structures are resonance contributors of the same species. The two structures are not resonance contributors because they contain different numbers of electrons. The two structures are not resonance contributors because they contain different bond orders. O The two structures are not resonance contributors because they contain bond orders having integer values. The two structures are not resonance contributors because each structure is present in its most stable (lowest energy) configuration. The two structures are not resonance contributors because they have different arrangements of atoms. X Ś2a) The molecule ethene (or ethylene), which has the molecular formula C₂H4, contains two carbon atoms with planar geometry. Construct a model of ethene by first connecting two black balls with two springs. Use four short sticks and four yellow balls to complete the structure. Sketch a perspective representation (a three dimensional drawing) of the structure. 2b) What is the C=C-H bond angle in ethene?
