Got #16 wrong, can you please explain.
Got #16 wrong, can you please explain. (B) SDS 16. Nucleophylic Substitution Leaving Group (A) -OH...
Got #12 wrong, can you please explain. (D) OH OH 12. Electrophylic Substitution Reactivity: HO. (A) (B) (C) (D) NO2 13. The Strength of Electrophile: (A) H NO. RA
Got #15 wrong, can you please explain. (1) TU 15. S Reactivity in Acetone: (A) Br (B) 16. Nucleophylic Substitution Leaving Group: A (C)- -NH
Got #11 wrong, can you please explain. OH (B) (B) (D) OH II. Solubility in Hexane: (A) OH 12. Electrophylie Substitution Reactivity
Got #17 wrong, can you please explain. 17. Polar Solvent 1 in Seremchemistry
I nucleophile substitution. 7.8 Which is the better leaving group in each pair? a a, b, NH, NH, C. HẠO, HAS 7.9 Which molecules contain good leaving groups? a. CH CH.CH,Br b . CH,CH,CH,OH . CH.CH,OH, d. CH.CH Does the equilibrium favor the reactants or products in each substitution reaction? a. CH,CH-NH, + Br -- CH,CHBr + NH b. n + ON ~ ON + r 7.6 Identify the nucleophile and leaving group and draw the products of each reaction...
Got this wrong, can you please explain. CIOOSE the compound which has a highest for each property: (question w9 9. Boiling Point: (A) (B) DH
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3. (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose the most appropriate solvent to facilitate...
got this wrong on my exam, can someone please explain how to get the answer? thank you 5 pts Is. Draw the products for the following reaction. Label then major ami minor + H2O miros
Explain how you got your answer please! What is the product of the nucleophilic substitution reaction shown below? None Only II I and II Only I
Please explain how you got the answer :) not necessarily additive!) and that group is given priority "1". What is the configuration at each of the indicated asymmetric centers in the structure below? C1H OH Η ΝΗ NH2 c2 C1 = R; C2 =R C1 = S; C2=5 C1 = 5; C2=R C1 =R; C2 = 5