O Answer all parts, please. 6) (10 pts) Provide the bond line structure for the major organic product formed in the reaction shown below. HO H₂O

(a) Compare the bond enthalpies (Table 8.3) of the carbon–carbon single, double, and triple bonds to deduce an averageπ -bond contribution to the enthalpy. What fraction ofa single bond does this quantity represent? (b) Make a similarcomparison of nitrogen–nitrogen bonds. What do youobserve? (c) Write Lewis structures of N2H4, N2H2, and N2,and determine the hybridization around nitrogen in eachcase. (d) Propose a reason for the large difference in yourobservations of parts (a) and (b).

Based on the atom connectivity shown bellow,evaluate the four resonance structure for the thiosulfate ion S2O3 ^2-. Use curved arrows to indicate how you get from one resonance structure to another. Assign formal changes to all atoms and determine which of these resonance structure is the most stable based on a formal charge analysis Explain your answer thoroughly. Look at the picture.

Draw a Lewis Structure for each of the following species and assign formal charge where appropriate. Using electronegative values from the period table that was provided identify polar covalent bonds and label the atoms δ+ and δ−. For each of the molecules indicate whether or not it has a dipole moment. (a)CH5N (b) HCN (c) H2CO (d) CH3NC(e) CH3SOCH3 (f) H6BN

(a) Determine the formal charge of oxygen in the following structure. If the atom is formally neutral, indicate a charge of zero. (b) Draw an alternative Lewis (resonance) structure for the compound given in part (a). Show the unshared pairs and nonzero formal charges in your structure. Don't use radicals. Formal charge on O 0

Draw a Lewis structure for each of the following                                        molecule:                                                     (a) chlorodifluoromethane, CHCIF2                                                               (b) propanoic acid C2H5CO2H (basic structure                                                  pictured below)                                                                                                                                                                                                                                                                                                                                                                                                                                                              (c) acetonitrile, CH3CN ( the framework is H3C-C-N)                                     (d) allene, H2CCCH2

The arrangement of atoms in several biologically important molecules is given here. Complete the Lewis structures of these molecules by adding multiple bonds and lone pairs. Do not add any more atoms. (a) the amino acid serine: 車 0-H H-C-H H Н—N—с—с—о—н H (b) нон H-N-C-N-H (c) pyruvic acid: ноо н—с—с—с—о—н H. (d) uracil: H (e) carbonic acid: H-0-C-0-H

Give correct detailed Solution with explanation needed..don't give Handwritten answer

Calculate the Enthalpy Change (ΔH) from average bond energies, which have been listed below in KJ/mol, for the following reaction and identify the nature of the reaction: CH3COOH + CH3OH → CH3COOCH3 + H2O [C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467]

A carbene is a compound that has a carbon bonded to twoatoms and a lone pair remaining on the carbon. Manycarbenes are very reactive. (a) Draw the Lewis structurefor the simplest carbene, H2C. (b) Predict the length of thecarbon–carbon bond you would expect if two H2C moleculesreacted with each other by a combination reaction.