5. Diazene is a compound with the formula N2H2 and is used in organic synthesis to...
Diazene N2H2 (also known as diimine), is commonly used as a reagent for organic syntheses. Label each picture with the type of bond in diazene that it describes.
Question #4 & #5?
3) Using Early and Late Molecular Orbitals, draw the two M.O. diagrams for NO , determine which is most stable; calculate and state bond order of each, state diamagnetic or paramagnetioc d if paramagnetic and by how many electrons. an 4) If four hydrogens, each with its 1s orbital, and two carbons, each with its one 2s and three 2p orbitals, form a molecule, then how many molecular orbitals will there be? How many bonding orbitals,...
2. The structure of the commonly used organic solvent dimethylformamide (DMF) is shown below. The numbers by each carbon atom are shown to distinguish each C atom in the molecule. Using Valence Bond Theory, answer the questions in parts a) and b). (4 pts) o: н LH H) N )H -Co HIH Dimethylformamide a) Specify the hybrid orbitals for each atom in the molecule indicated below C 2): N: C(1): b) Identify the bond type(s) and the overlapping orbitals of...
V. (1.5 points) 1. For the following compound identify the polar covalent bonds and indicate the direction of dipole moment using 8+ and 8-. Of the polar bond you have selected, circle the mot polar bond. (0.75 point) H H 2. Indicate the atomic/hybrid orbitals that are involved in the formation of each o (sigma) and TT (pi) bond, in the following compound. The lone pairs of electrons of the nitrogen and oxygen atom are located in which orbitals? (0.75...
Draw a sketch of the hybrid orbital/atomic orbitals for the molecules below, including orbitals used for bonds, lone pairs, and empty orbitals. Dont forget to include the phase of the orbitalsusing shading. Label each hybrid or atomic orbital. Also draw the MO diagram indicate the HOMO and LUMO. a. CH3CH2+ b. CO
9. Consider the shorthand structure below (which also does not show lone pair electrons on N, O, or S). H N S YX -ОН (a) (5 pts each) Fill in the correct number next to the atomic symbol, for the molecular formula of this compound. H = C = N = S = (b) (5 pts each) For each of the atoms indicated by a, b, c, indicate the hybrid atomic orbitals you would expect it to be using to...
9. Consider the shorthand structure below (which also does not show lone pair electrons on N, O, or S). н. S YX N OH (a) (5 pts each) Fill in the correct number next to the atomic symbol, for the molecular formula of this compound. H = C = N = S = (b) (5 pts each) For each of the atoms indicated by a, b, c, indicate the hybrid atomic orbitals you would expect it to be using to...
9. Consider the shorthand structure below (which also does not show lone pair electrons on N, O, or S). Н. N S I 11 -N OH (a) (5 pts each) Fill in the correct number next to the atomic symbol, for the molecular formula of this compound. H= C= N = S = (b) (5 pts each) For each of the atoms indicated by a, b, c, indicate the hybrid atomic orbitals you would expect it to be using to...
9. Consider the shorthand structure below (which also does not show lone pair electrons on N, O, or S). H S X S = -ОН (a) (5 pts each) Fill in the correct number next to the atomic symbol, for the molecular formula of this compound. H= C= N = (b) (5 pts each) For each of the atoms indicated by a, b, c, indicate the hybrid atomic orbitals you would expect it to be using to bond. a= b=...
9. Consider the shorthand structure below (which also does not show lone pair electrons on N, O, or S). Н. -S OH O (a) (5 pts each) Fill in the correct number next to the atomic symbol, for the molecular formula of this compound. H = C= N = S = (b) (5 pts each) For each of the atoms indicated by a, b, c, indicate the hybrid atomic orbitals you would expect it to be using to bond. a...