ouro- 6)- Draw the structures for the least and most polar molecules (i.e.,isomers) of Bromo-chloro-fl iodoethene (C2BrCIFI). Briefly explain your choice. Structure of least polar: Structure of most polar:
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- 1 ethel 2 isopropylcyclohexane Which structure would be most stable cis?What are all of the types of orbital overlaps that occur in the above structure. p-p overlap sp²-sp overlap s-sp² overlap sp²-sp² overlap s-sp overlap sp-sp overlap s-s overlap ---------- In cumulene, what are the C=C=C and H−C−H ideal bond angles, respectively?Enter the C=C=C bond angle followed by the H−C−H bond angle separated by a comma (no spaces, no º symbol required).draw bond-line structure for 3-ethylbicyclop<3.2.1>octane?
- Which molecule would be more polar, CH3F or CH3Cl? And why?I'm confused by the (CH3)2 at the final step. is there supposed to be a - connecting it? What is the name of the molecule? I've never seen a structure written like thatMake a continuous model for C4H10 by using 4 black 4 hole carbon atoms, 10 white one hole hydrogen atoms, and 13 pink bonds. Then write in wedge dash notation C4H10 and add in missing hydrogen atoms.
- Rank each of the representations of NOCl from best to worst, placing the best structure on top and the worst at the bottom.I need to know the names of these two structurers for my notes but I am not sure how to name them.Construct the three-dimensional model of 2-methylhexane, also draw the anti and gauche models where the rotation between carbons 3 and 4 is clearly appreciated.
- What are the features of Radicals, Carbocations, and Carbanions ?How would I draw all the important resonance structures for cyanate (NCO1-)?Draw the molecular orbital diagram of a linear C-H (i.e. one carbon atom bonded to one hydrogen atom). Draw out the MOs for orbitals containing electrons. 1. Would you expect C-H to behave as a carbocation, carbanion, or radical? 2. Would removal of one electron from C-H to generate C-H+ increase or decrease the bond length between carbon and hydrogen?