What is the hybridization of the carbon atom indicated with a star in the given structure? Br show work. don't give Ai generated solution sp2 sp3

Consider acetyl salicylic acid, better known as aspirin. Its structure is (a) How many sigma and pi bonds are there in aspirin? (b) What are the approximate values of the angles marked (in blue) A, B, and C? (c) What is the hybridization of each atom marked (in red) 1, 2, and 3?

Consider the following flat drawing of methane (CH4) . a. What is HCH bond angle implied by this drawing if you assume it is flat? b. Are the electron domains of this flat CH4 spread out as much as possible? c. Use model materials to make a model of CH4 (methane). If you assembled it correctly, thefour bonds (bonding electron domains) of your model will be 109.5° apart. d. In which representation, the drawing above or the model in your hand (circle one) are theH’s of CH4 more spread out around the central carbon? e. Confirm that your model looks like the following drawing. The wedgebond represents a bond coming out of the page, and the dash bondrepresents a bond going into the page f. You will often see methane drawn as if it were flat (like on the previous page). Why is thismisleading, and what is left to the viewer’s imagination when looking at such a drawing?

When two amino acids react with each other, they form a linkage called an amide group, or a peptide link. (If more linkage. are added, a protein or polypeptide is formed.) (a) What are the hybridizations of the C and N atoms in the peptide linkage? (b) Is the structure illustrated the only resonance structure possible for the peptide linkage? If another resonance structure is possible. compare it with the o ne shown. Decide which is the more important structure. (c) The computer-generated structure shown here, which contains a peptide linkage, shows that this linkage is flat. This is an important feature of proteins. Speculate on reasons that the CONH linkage is planar. What are the sites of positive and negative charge in this dipeptide?

Strike-anywhere matches contain a layer of KClO3 and a layer of P4S3. The heat produced by the friction of striking the match causes these two compounds to react vigorously, which sets fire to the wooden stem of the match. KCIO3 contains the ClO3 ion. P4S3 is an unusual molecule with the skeletal structure. (a) Write Lewis structures for P4S3 and the ClO3 ion. (b) Describe the geometry about the P atoms, the S atom, and the Cl atom in these species. (c) Assign a hybridization to the P atoms, the S atom, and the Cl atom in these species. (d) Determine the oxidation states and formal charge of the atoms in P4S3 and the ClO3 ion.

Determine the bond order of each member of the following groups, and determine which member of each group is predicted by the molecular orbital model to have the strongest bond. (a) H2,H2+,H2 (b) O2,O22+,O22 (c) Li2,Be2+,Be2 (d) F2,F2+,F2 (e) N2,N2+,N2

Minoxidil (C9H15N15O) is a compound produced by the Pharmacia Upjohn Company that has been approved as a treatment for some types of male pattern baldness. Note that in such shorthand ring structures, each point where lines meet is a carbon atom and that the hydrogen atoms bonded to the carbon atoms in the rings have been omitted. There will be four bonds to each carbon atom. a. Give the hybridization of the five nitrogen atoms in minoxidil. b. Give the hybridization of each of the nine carbon atoms in minoxidil. c. Give the approximate values for the bond angles marked a, b, c, d, e, and f. d. Including all the hydrogen atoms, how many bonds exist in minoxidil? e. How many bonds exist in minoxidil?

The molecular orbital diagram of NO shown in Figure 10.47 also applies to the following species. Write the molecular orbital electron configuration of each, indicating the bond order and the number of unpaired electrons. (a) LiBe+ (b) CO+ (c) CN (d) OF Figure 10.47 Molecular orbital diagram for nitric oxide (NO). The molecular orbital diagram for NO predicts a bond order of 2.5 and predicts that the molecule is paramagnetic with one unpaired electron. These predictions are verified by experimental measurements.

• explain how hybridization reconciles observed molecular shapes with the orbital overlap model.

The uracil molecule is one of the bases in DNA. Estimate the approximate values of the indicated bond angles. Its skeleton (not its Lewis structure) is given below.