Can someone explain how to convert a condensed formula to a bond. I get confused about atoms that aren’t C or H and when to branch . Thanks for any explanation

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?

A compound of chlorine and fluorine, CIFx, reacts at about 75C with uranium to produce uranium hexafluoride and chlorine fluoride, CIF. A certain amount of uranium produced 5.63 g of uranium hexafluoride and 457 mL of chlorine fluoride at 75C and 3.00 atm. What is x? Describe the geometry, polarity, and bond angles of the compound and the hybridization of chlorine. How many sigma and pi bonds are there?

Which of the following statements is/are true? Correct the false statements. a. The molecules SeS3. SeS2, PCl5, TeCl4, ICl3, and XeCl2 all exhibit at least one bond angle which is approximately 120. b. The bond angle in SO2 should be similar to the bond angle in CS2 or SCI2. c. Of the compounds CF4, KrF4, and SeF4, only SeF4 exhibits an overall dipole moment (is polar). d. Central atoms in a molecule adopt a geometry of the bonded atoms and lone pairs about the central atom in order to maximize electron repulsions.

What are the bond angles predicted by the VSEPR model about the carbon atom in the formate ion, HCO2? Considering that the bonds to this atom are not identical, would you expect the experimental values to agree precisely with the VSEPR values? How might they differ?

Use Figs. 4-54 and 4-55 to answer the following questions. a. Would the bonding molecular orbital in HF place greater electron density near the H or the F atom? Why? b. Would the bonding molecular orbital have greater fluorine 2p character, greater hydrogen 1s character, or an equal contribution from both? Why? c. Answer the previous two questions for the antibonding molecular orbital in HF.

The ions ClF2 and ClF2+ have both been observed. Use the VSEPR model to predict the FClF bond angle in each.

Compare Figs. 4-47 and 4-49. Why are they different? Because B2 is known to be paramagnetic, the 2p and 2p molecular orbitals must be switched from the first prediction. What is the rationale for this? Why might one expect the 2p to be lower in energy than the 2p? Why cant we use diatomic oxygen to help us decide whether the 2p, or 2p, is lower in energy?

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What atomic or hybrid orbitals make up the sigma bond between C2 and H in ethane, CH3CH3 ?(C2 is the second carbon in the structure as written.)  orbital on C2 +  orbital on H What is the approximate C1-C2-H bond angle ? ... fill in the blank 3 °