Chapter 1: Problem 46
Draw structural formulas for the three tertiary \(\left(3^{\circ}\right)\) amines with the molecular formula \(\mathrm{C}_{5} \mathrm{H}_{13} \mathrm{~N}\).
Chapter 1: Problem 46
Draw structural formulas for the three tertiary \(\left(3^{\circ}\right)\) amines with the molecular formula \(\mathrm{C}_{5} \mathrm{H}_{13} \mathrm{~N}\).
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Get started for freeFollowing are three contributing structures for diazomethane, \(\mathrm{CH}_{2}
\mathrm{~N}_{2}\). This molecule is used to make methyl esters from carboxylic
acids (Section 17.7C).
In Chapter 6, we study a group of organic cations called carbocations. Following is the structure of one such carbocation, the tert-butyl cation. (a) How many electrons are in the valence shell of the carbon bearing the positive charge? (b) UsingVSEPR, predict the bond angles about this carbon. (c) Given the bond angle you predicted in (b), what hybridization do you predict for this carbon?
Using cartoon representations, draw a molecular orbital mixing diagram for a \(\mathrm{C}-\mathrm{O}\) \(\sigma\) bond. In your picture, consider the relative energies of \(\mathrm{C}\) and \(\mathrm{O}\) and how this changes the resulting bonding and antibonding molecular orbitals relative to a \(\mathrm{C}-\mathrm{C} \sigma\) bond.
Describe each highlighted bond in terms of the overlap of atomic orbitals.
(a)
Define valence shell and valence electron.
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