AICI 3. (15 points each) Predict the products and present a detailed mechanism for the following reactions. If an intermediate is stabilized by resonance, draw all resonance structures. Show all lone pair electrons and label any charged atoms.
Predict the products anticipated for the following reactions; 1. EtMgBr/THF 2. NH C/ H2O a. 1. n-BuLi, Et2O 2. NH CI, H2O b. H KCN, HCI C. NaCN, HC d.
Lecture Questions Determine if each of the following reactions is Sn1 or SN2. Then predict the products: L Nao OTS H20 heat Nao NaOH O- Exit ft I D 1:52 / 6:17 CC acer
Predict the products of the following reactions.
a.
b.
c.
(1) excess CH Mg! CI (2) H30* (1) DIBAL-H (-78 °C) (2) H30 OCH (1) DIBAL-H (-78 °C) (2) H2O
predict the major products obtained from each of the following reactions and show the stereochemistry where pertinent. NaNH2 1 ) 2) H30 H2, Pd/BaSO4 OsO4 Quinoline NMO NH3 1) MCPBA Na 2) H3o
Predict the products of each of the following reactions: 1. HNO3 (aq) KOH (aq) 2. HNO3 (aq) + (CH3)&N 3. HNO2 (aq) + NaOH > List the salts produced in the above reactions:
please help with the following question (a-f).
6-95. Predict the diene and dienophik that would lead to each of the following products CFs (al (ci le) CH1 CCH, CH CO.CH, tb) (dl 10D CO,CH,
CONCEPTUAL CHECKPOINT 13.10 Predict the products for each of the following reactions O Excess oExcess Excess HBr Heat HI Heat HBr Heat O Excess Excess HI Heat Excess HI Heat HBr Heat
please help! thank you
47) Draw out the reaction mechanism for a Fischer esterification reaction with ethanol and benzoic acid in hot acidic conditions. Name the products. 48) Draw out the reaction mechanism for a Fischer esterification reaction when 5-hydroxyhexanoic acid is heated. Name the products if you feel ambitious.
Predict the product of the following reaction sequence. i. NaOet, EtOH ii. NaOH, heat iii. H20" iv. heat YOH O