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- nost" under the one which nder the one which would be acetaldehyde e "most" under the one which would be most t" under the one which would be least soluble in wa formaldehyde butanal Write in the products. Label "major" and "minor" products where relevant. If there is no reaction, write "NR". a) H3C- он H3C H,SO, heat -CH3 b) CH3 1. Hg(Oac), H,0 2. NABH, H3O* --- > c) hexanal d) HO CH3 KMNO, CH3 NaHWhich alkene is LEAST reactive in acid-catalyzed hydration? all have equal reactivity А. В. c. D. Е.Click the "draw structure" button to launch the drawing utility. Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H,0, H,SO,, and HgSO,? Draw the second ketone formed from these enols after tautomerization. H2O H2SO, H9SO, + Product A Product A = draw structure...
- Reagent Table Dicyclopentadiene Cyclopentadiene Maleic Anhydride Ethyl Acetate Hexanes cis-norbornene-5,6- endo-dicarboxylic anhydride Melting Point (°C) N/A N/A N/A N/A Boiling Point (°C) N/A N/A Density (g/cm³) Solubility in Water Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Table view Choose... Choose... ✓ Choose... Liquid Organic Waste Bottle Solid Chemical Waste Bucket Sink with Copious Water Choose... Choose... Choose... Choose... List view Choose... Choose... Disposal1. 2-bromobutane + cyclohexanol + NaH à (major product) c. 2-butoxycyclohexane a.. 2-butene reaction b. 1-butene d. no e. something else! 2. t-butylbromide + sodium ethoxide in ethanol à (major product) a. 2-methylpropene reaction b. t-butyl ethyl ether c. 1-methylbutene d. no e. something else! 3. potassium t-butoxide + 1-bromobutane in t-butyl alcohol room temperature à (major product) a. 1-butene reaction c. 2-methylpropene d. no b. butyl t-butyl ether e. something else! 4. t-butyl bromide + boiling hot water à (major product) a. 2-methylpropene reaction b. t-butyl ethyl ether c. t-butanol d. no e. something else! 5. 2-chloropropane + acetic acid (2 eq) / KOH (1 eq) / DMF à(major product) c. b. d. no reaction e. something а. HO. else! Br KOH / DMSO 6. b. 2-methyl-1-propanol d. 1,2- a. 2-methylpropene propanediene c. no reaction e. something else! 7. cyclopentanol+ NaH + DMSO + bromopropane à(major product) a. cyclopentene reaction b. propene e. something else!! c. propyl cyclopentyl…- Draw the structural formula of compounds K, I, L and J.- Reagents for M and N.
- True/False question and multiple choice. explanatiom not needed. just give the answer. thank you. a) Williamson synthesis of ether requires un hindered alkyl halide and hindered alcohol b) NaBH4 can reduce a carboxylic acid to primary alcohol c) Conjugated diene reacts with which among the following to form a cyclohexene?1) Phenol2) Dienophile3) Hexane4) Tribromo phenol d) 1,3 -cyclohexadiene is 1. aromatic 2. has higher heat of hydrogenation than cyclohexene 3. is a good dienopile 4. has lower heat of hydrogenation than cyclohexeneAcyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?2. formed. a. b. ) Predict the major organic product(s) for the following reactions. Draw all stereoisomers H₂SO4 CH3OH HBr
- 1. Nomenclature a. (E)-5-chloro-3-hexen-2-one b. 3-bromopentanal c. 4-bromoacetophenone d. 3-sec-butyl-5-isopropylcyclohexane carbaldehyde ii) Hexanedial from cyclohexane f. iii) 1-bromo-1-methylethyl 1-chloroethyl ether 8. h. OH Ila. Carry out the following conversions 5X1.5-7.5 pts (any 5 of 6 (IIa.i-IIa.vi) 3-chloro-2,4-hexanediol 2Provide the missing reagents/product thnksAcyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous Next