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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- I know that the answer to this question is 60, but I am struggling to understand why. Could somebody please draw this out for me 3-dimensionally or explain to me in detail why this is the case? One explanation I've heard is that it is because when the dihedral angle between the two methyl groups is 60, the molecular dipole moment between the two chlorine atoms is the smallest, therefore the answer is 60. This explanation is meaningless to me - that does not even seem to be what the question is asking. Is it a poorly-worded question? i need good explanationCTQ 7: Why is it incorrect to describe the process of boiling as 2H,0(1) → 2H,(g) + 0,(g)?Select the bonds in the 3D representation of methyl urethane below that are multiple bonds. (Hint: Consider the number of bonds attached to an atom in the image compared to the normal valence of that atom. In a valid structure, the number of bonds to an atom will equal the valence of that atom.) • Gray = C: white = H; red = 0; blue = N; dark green = Cl; brown = Br; light green = F; purple = 1; yellow = S: orange = P. • Double click to select bonds. You can zoom in and out using the mouse scroll wheel (or pinch to zoom on touch screens). ●
- Please don't provide handwritten solution ....These two different C2H6O compounds are called structural (or constitutional) isomers - compounds with the same molecular formula but with different connections among their constituent atoms. If you must break and make new bonds in order to convert one structure into the other (not simply rotate the model around), then they are structural isomers. The concept of isomers is very important in organic chemistry and biochemistry. This is also another instance where condensed formulas can be very useful because they can help you distinguish two isomers apart even when you don't have models. Exercise 8) Can your models be interconverted by rotating bonds, or must the bonds be broken first? What does that mean about these two structures?Help answer the following question, give one biological example of where shape determines function and one non biological example.
- 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 PMFor the molecular formula CH3NO: Draw a valid Lewis structure, showing all lone pairs of electrons. Draw a second, valid, and distinct Lewis structure from the first, again showing all lone pairs 1) 2) For each structure you drew, indicate which bond is most polar, and provide your reasoning. You should look up Pauling electronegativity values to answer this question. 3) For the bond you chose as the most polar in each structure, provide a molecular orbital description (not diagram!) of the bonding orbital overlaps. 4) For each structure you drew, indicate the hybridization of the carbon atom, the nitrogen atom, and the oxygen atom. 5) For the carbon atom in each structure, what is the hybridization? What is the shape around that carbon atom?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 carbon
- Use 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.thx!
