need help answering question 1, 6 and 7.

1. Consider the following life saving molecules. Give all the missing electrons, circle, and name all the functional groups. State for what medications each of these molecules are used for. (3 points) 2.Using curved arrows write the resulting resonance structures for the given molecules. Must include all formal charges in the products as well ( 3 points) (a) (d) (b) (e) (c) (f) 3.Complete the following acid base reactions. Must draw all curved arrows, give Pka values of acids and conjugate acids. (3) points (a) HC=CH+NaHnexane (b) The solution obtained in (a) +D2O (c) CH3CH2Li+D2O hexane (d) CH3CH2OH+NaHnoxane (e) The solution obtained in (d) +T2O (f) CH3CH2CH2Li+D2O exane 4.Select the stronger base in each of the following compounds. Write the pka of each of the conjugate acids ( 3 points) (b) (CH3)iCO2 of 5. Write the bond line structures of the following (3 point). Indicate primary, secondary, and tertiary (a) Isobutyl Alcohol (C) Neopentyl Bromide (b) Isopropyl Chloride. (d) Tert Butyl Amine. (c) isopentyl alcohol (d)sec butyl chloride. 6. Consider the molecule: FCN. (3 points) (a) Draw all possible resonance structure(s) including all formal charges. Indicate the most stable and least stable one. (1) point) (b) For the most stable Lewis structure you have drawn in (6a), Show hybridization and construct the orbital picture of the molecule. Must label each of the overiap of orbitals that resulted in the formation all sigma and pi bonds with each atom in the molecule (2) points) 7. (a) Using curved arrows and write the reaction to show what happens when Sudafed reacts with water in the human body. (1 point) (b) Explain keto enol tautomerization in acetyl acetone (CH3COCH2COCH3). Draw Lewis structures with appropriate arrows. (1pt) 1. Consider the following life saving molecules. Give all the missing electrons, circle, and name all the functional groups. State for what medications each of these molecules are used for. (3 points) 2.Using curved arrows write the resulting resonance structures for the given molecules. Must include all formal charges in the products as well ( 3 points) (a) (d) (b) (e) (c) (f) 3.Complete the following acid base reactions. Must draw all curved arrows, give Pka values of acids and conjugate acids. (3) points (a) HC=CH+NaHnexane (b) The solution obtained in (a) +D2O (c) CH3CH2Li+D2O hexane (d) CH3CH2OH+NaHnoxane (e) The solution obtained in (d) +T2O (f) CH3CH2CH2Li+D2O exane 4.Select the stronger base in each of the following compounds. Write the pka of each of the conjugate acids ( 3 points) (b) (CH3)iCO2 of 5. Write the bond line structures of the following (3 point). Indicate primary, secondary, and tertiary (a) Isobutyl Alcohol (C) Neopentyl Bromide (b) Isopropyl Chloride. (d) Tert Butyl Amine. (c) isopentyl alcohol (d)sec butyl chloride. 6. Consider the molecule: FCN. (3 points) (a) Draw all possible resonance structure(s) including all formal charges. Indicate the most stable and least stable one. (1) point) (b) For the most stable Lewis structure you have drawn in (6a), Show hybridization and construct the orbital picture of the molecule. Must label each of the overiap of orbitals that resulted in the formation all sigma and pi bonds with each atom in the molecule (2) points) 7. (a) Using curved arrows and write the reaction to show what happens when Sudafed reacts with water in the human body. (1 point) (b) Explain keto enol tautomerization in acetyl acetone (CH3COCH2COCH3). Draw Lewis structures with appropriate arrows. (1pt)