Assign a hybridization to each interior atom in guanine.

Describe each highlighted bond in terms of the overlap of atomic orbitals. (If the highlighted bond is not a pi bond, select the blank option from the dropdown menu.)

For each of the following condensed structures: (i) draw the corresponding Lewis structures and (ii) provide the hybridization to all carbon atoms; (iii) draw individual p orbitals for all the π bonds with directions clearly indicated. a) CH2CHCHCH2 b) CH3CCCH3 c) CH2CCHCH3

Please help, a bit conufsed

2) a) Consider the following molecule . Given what you have learned about hybridization theory, draw an image or images explaining the bonding situation in this molecule. I want you to draw out all of the orbitals, hybrid orbitals and how they overlap to form the bonds in the molecule. Indicate the % s or p character in the given atomic and hybrid orbitals. Which C-C bond or bonds are the longest? In a paragraph or so explain the image or images you just drew. b) Lastly, consider the molecule below. Indicate the Molecular formula, the molar mass, label the hybridization of each atom except for hydrogen, indicate any chiral centers with a *, which bond or bonds are the shortest, identify by name of each functional group with an arrow pointing to the group.

a) Consider a molecule of acetone cyanohydrin, shown below. What is the hybridization and molecular geometry at CA, CB, and O?  (b) For Carbon B (CB) and nitrogen (N), draw orbital energy diagrams showing the orbitals involved in bonding after hybridization. Be sure to fill the orbitals appropriately with valence electrons. c) In your diagrams in part (b), which orbitals are involved in sigma and pi bonding?            Orbitals Involved in Sigma Bonding                                       Orbitals Involved in Pi Bonding  2p sp sp2 sp3 2p sp sp2 sp3 (d) In a sample containing many molecules of acetone cyanohydrin (and no other substances), what type(s) of intermolecular forces could be present? Choose all that apply. Covalent Bonds            Hydrogen Bonds              Dipole-Dipole Forces              London Dispersion Forces