9. Plan syntheses of the following compounds. You may use compound containing three or fewer carbons. "bg" H (a) (b) (c) (d) Br Br Br H 1 OH == OH
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- 8. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) (b) (c) NH₂ sef= -OH11. Plan syntheses of the following compounds. You may use the given starting material and any compound containing five or fewer carbons. (a) MeO MeO CN TOXXON anything with five or fewer carbons. CN (b) (c)6. Write the IUPAC name for the following compounds. Show the stereochemistry whenever required (a) HO NH2 CI (b) NH2 QH но (c) он Br H. (d) (e) OH Br Br
- 9. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) OH (b) Br Br- (c) ✓ -OTS (d) OH10) What is the major product? (A) (C) OH (B) H₂SO4 (cat) H₂O (D) НО. ОН .4. What product is expected from this reaction? (A) (C) N. NH₂ OH -NHNH2 NHANH2 (B) (D) NH NH₂ f NH₂
- Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3 (c) CH3CH2COCl, AlCl3(d) isobutylene and HF1. At what position and on what ring would you expect the following substances to undergo electrophilic substitution? (b) CH3 Br lel CH3 2. Rank the compounds in each group according to their reactivity toward electrophilic substitution. (a) Chlorobenzene, o-dichlorobenzene, benzene (b) p-Bromonitrobenzene, nitrobenzene, phenol (c) Fluorobenzene, benzaldehyde, 0-xylene (d) Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrileDraw the structure of the organic product formed when 2,3-butanedione reacts with the following reagents. CH3 -C-C-CH3 | (a)H2/Ni (b)l2/NAOH 3D
- 1) Provide the reagent(s) and the reaction mechanism of the following reaction. H₂NElectrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3 (c) CH3CH2COCl, AlCl3Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4