Chapter 2, Problem 56P

Resonance Formsa) Draw all resonance forms of the molecules. Include curved arrow notation. Label majorresonance contributor.

Show work with explanation needed. Don't give Ai generated solution

f) The unusual molecule [2.2.2] propellane is pictured. 1) Given the bond length and bond angles in the image, what hybridization scheme best describes the carbons marked by the askerisks? 2) What types of orbitals are used in the bond between the two carbons marked by the askerisks? 3) How does this bond compare to an ordinary carbon-carbon bond (which is usually 1.54 Å long)? CH2 1.60Å H2C た C CH2 H2C H₂C * 120° C H2

Denote the dipole for the indicated bonds in the following molecules. H3C CH3 B F-CCl3 Br-Cl | H3C Si(CH3)3 OH НО. HO H O HO OH vitamin C CH3

Q2: Draw all applicable resonance forms for the acetate ion CH3COO. Clearly show all lone pairs, charges, and arrow formalism.

How do I calculate the amount of quarks in magnesium?

Please provide the mechanism for the reaction attached. Please include all arrows, intermediates, and formalcharges. If a Sigma complex, please draw all major resonance forms.

Predict the product or products for the following reactions. Please include both ortho and para substitutions, if it applies, and indicate the major product, if it applies.

The bromination of naphthalene via electrophilic aromatic substitution. Please draw out all of the resonance structures created from addition at the C1 carbon. Please also draw out all of the resonance structures created from addition at the C2 carbon. Which carbon (C1 or C2) is more favored?