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- TReferences] Indicate, by letter(s), the position(s) on the ring at which substitution occurs when the aromatic compounds shown undergo bromination with Br, FeBr3 (when necessary). .H CN HON(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reactionapp.101edu.co oudy @ 2 X V * UL Week 7: Panopto ||| 3 D E PII $ 4 R Rank these alkyl halides in order of increasing reactivity in an SN2 reaction. F 4x X UL LTU 7-1A F4 HHH % 5 T G 4, CI F5 A 6 4) Y X Question 16 of 24 F6 C|Chegg.com & 7 U F7 ★ A) III < | < || 8 B) || < | < ||| C) ||| < || < | D) || < ||| < | E) | < ||| < || PrtScn 1 FB X + Home ( 9 F9 O ) End 0 D 67 ENG F10 P PgUp Tp S ( D [ * O 6:15 PM 10/18/2022 PgDn + F12 0 SL 3
- What is the major substitution product to the following reaction? Но OCH,CH3 Chapter 9 Homew..pdf IMG_4217 (1)jpeg MG 4217jpeg IN4. What are the products obtained from the following elimination reaction? Indicate the major product. CH;CH2CCH3 H2O CI 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion in an elimination reaction. CH;CH,CH,CH,CCH3 Br b) For the major elimination product obtained in 5a), which stereoisomer (cis or trans) is obtained in greater yield? Draw the two isomers and provide the names of the compounds.Determine the major product of the rxn O Li" -Н20 1. ? OH- heat 2. H2O a. b. C. d.
- 12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CI6. What are the line structures of compounds E and F in the following sequence of reactions? 0 Compound E L NINH,NH, 2. CH₂CH₂Br Compound F H₂O, H₂SO₂ HgSO; CH₂CH₂CCH₂CH₂CH₂R'R?CHOH-CR°R* R'R?C=CR®R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?
- R'R°CHOH-CR'R* R'R?C=CR*R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?Q, - write a Mechanism that explains hint he stereochemisty (sed pmacal rearangemendy a) CotH6 fonn Hcl b) HeoH O wr,te he Mechanism fer OH CHBrg NAOH (Carbene)CH3 CH3 CH3 CH;=ĊCH,CHCH;OH H2SO4, H3C H3C Referring to the above reaction: 1. Which atom does the H2SO4 first remove? 2. Identify the reaction if it's hydrogenation, hydrohalogenation, etc. 3. Propose a mechanism for the reaction, using the arrow formalism to indicate the flow of electrons.