Got #15 wrong, can you please explain.
Got #15 wrong, can you please explain. (1) TU 15. S Reactivity in Acetone: (A) Br...
Got #16 wrong, can you please explain. (B) SDS 16. Nucleophylic Substitution Leaving Group (A) -OH (B) —F 17. Polar Solvent:
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 #11 wrong, can you please explain. OH (B) (B) (D) OH II. Solubility in Hexane: (A) OH 12. Electrophylie Substitution Reactivity
14. SNİ Reactivity in a Protic Solvent: CI (D) Br 15. SN2 Reactivity in an Aprotic Solvent: Br 16. Electrophylic Substitution Reactivity (B) c C) (D) Br- но 17. Polar Solvent он 18. Priority Group in Stereochemistry: (A) -NO2 (C) SH (D)) -SO,H (B) -OH 19. The Strength of Oxidizer: (A) PCC (B) H2SO4 (C) KMno,/H,SO (D) HNO
15. Rank in order of Sn2 reactivity (1- most reactive) 16. Rank in order of leaving group ability (1- best leaving group) NH2 H20 CI 17. For each reaction, give the expected substitution product, and predict whether the mechanism will be predominantly first rder or second order. (a) 2-chloro-2-methylbutane CH3COOH (b) cyclohexyl bromide+ sodium ethoxide 18. Provide clear mechanism for the following reaction: CH2OCH3 Br CH3OH +HBr
Got #17 wrong, can you please explain. 17. Polar Solvent 1 in Seremchemistry
3. Give the order of reactivity of the alkyl halides you reacted with aqueous silver nitrate. Does this ordering match what you would expect based on the alkyl group? Explain. Does this ordering match what you would expect based on leaving group? Explain. (To decide, you must compare only the three primary halides. Comparing a primary bromide with a tertiary chloride, for example, will not give a valid comparison of leaving groups as the substitution is also different.) 4. Give...
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
are these correct? if not, can you explain? thanks! 6. Rank the following, with 1 being highest/most. (2 points each, 16 points) Stability Stability Heat of Hydrogenation Reactivity towards Cl2 addition (No Lewis acid, no hv) d. 2 Br Reactivity towards Sn2 attack by NaOCH, H H - Br I Br Cation Stability. (Remember that other resonance structures also pertain and impact the overall stability of the cations.) Br Насо 3 Reactivity towards reaction with cyclopentadiene Reactivity towards Sn1 substitution...
Can someone please explain why I got the ones with a red mark wrong? I had to pick R vs S to chiral centers. please write ledgibly, thank you. for the first molecule, it has to be an R because O has bigger atom mass than N? I am so confused. thank you in advance SR RRR Cholesterol c) H