MATCH each definition to the term it describes. Place the letter corresponding to the term in the blank to the left of the definition. (17-20) a. Hammond Postulate b. Cahn-Ingold-Prelog Rules c. Markovnikov's Rule 17. alkenes. don't give Ai generated solution predicts that the more stable carbocation intermediate is formed in electrophilic additions to 18. reactant. predicts that the transition state of an exergonic reaction step structurally resembles the 19. 20. product. assigns priorities to the substituent groups on a carbon. predicts that the transition state of an endergonic reaction step structurally resembles the

Answer number 19, 20, and 21.

7.

What would be the effect on the rate of reaction if the concentration of the nucleophile weredoubled in an…a. SN1 reaction? Briefly explain.b. SN2 reaction? Briefly explain.

for this question. Draw a structural formula for the missing product in the following reaction. 0. NaHCO3 H20 ? + CO2 + H20 + CH3C-OH • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. C P. opy aste [F **** C - Visited CH4 ChemDoodle Retry Entire Group 5 more group attempts remaining Submit Answer

[References] Use the References to access important values if needed for this question. Draw the structure of the organic product that is expected when the following compound is treated with concentrated H,SO4. CH3 CH2CCH2CH3 tosH heat HO. • You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ed P. opy aste C. CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and

Please answer parts i and j

URGENT!!I will rate, pls need this. no need of long explanation.

To preview image Click Here Provide the missing major organic products, pay attention to stereochemistry as appropriate. B. C. D. E. Br OH CI 1 CHÍNH 2. LIAH, 3. H₂O* H₂O* 1. Mg/THF 2. CO2 3. H₂O 1. Excess MeMgBr 2. H₂O* 1. SOCI₂ 2. =O OH

Electron pairs CH3 .. Erase H3C - С — СІ: H3C – S- CH3 CH3 CH, CH3 THF/H,0 + H,C--CH, CH C- CH CHs CH, Use curved arrows to write the first step of this nucleophilic substitution mechanism. :ö: | :ö: