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2. (10 pts) Draw structures of the following alkynes: a) 5-isopropyl - 2 - heptyne b)...
Draw structures corresponding to the following names: 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne 9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
Help please Draw the following alkynes: 4-bromo-3, 3-diethylhex-i-en-5-yne 3, 10-dimethy-6-secbutylcyclodecyne) 1, 3-hexadien-5-yne s-ethyl-s-methyl-1.6.8-decatriyne Z-5, 7-dimethyl-4-octen-1-yne
Draw the structure of the following compounds (2 pts ca.) 5. 2-pentyne 72,5-diethyl-3-octyne 6. 3-ethyl-4,6-dimethyl-1-heptyne 8. 3.4.4-trimethyl-1-pentyne
(10 pts) 5. The molecule isopropyl ethyl ether is a good solvent for S.2 reactions. Draw isopropyl ethyl ether. Let's say you need an 5.2 solvent other than THF. You have significant quantities of isopropyl alcohol (rubbing alcohol) and ethanol (vodka) in your basement. You also have THF, ether, pyridine, DMSO, H., Mg, TSCI, NaBr, NaH, and KOrBu. Show how you would make isopropyl ethyl ether. If you use a reaction that makes multiple products, be sure to list them....
Provide structures for the following: 4,4-dimethyl-2-pentyne 5,5-dimethylnon-3-yne 4,5,5-trimethyl-2-hexyne 1-penten-4-yne 1-cyclohexylethyne propyne 4-isopropyl-2-methyl-1-nonene 6-ethyl-3-nonyne
Draw bond line structures for the following: 1,1,3-triethylcyclooctane 4,5-diethylnonane 1-butyl-3-fluorocyclobutane 4-ethyl-3-isopropyl-2-methylhexane
2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3. 2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3.
5. Draw structure for the names and write the IUPAC name for the structures to points) Tho priority of functional groups for naming is: alkane < alkyl halide <ether <alkene alkyne < amine < alcohol ketone <aldehyde <carboxylic acid NH2 a. 3-chloro-4,4-dimethyl-1-nonen-6-yne d. (3E, 5Z)-2,6-Dimethyl-1,3,5,7-octatetraene
Page of 11 1. Draw structures for the following molecules: ZOOM 5, 5-dimethyl-3-hepten-1-al 2-amino-3-isopropyl-1-butanoic acid 2, 4, 6-tribromo-1, 3, 5-trinitro cyclohexane 3-methoxy-2, 5-hexanedione N-ethyl-N, N-dimethyl amine 3, 4-dihydroxy-1, 6-hexanedioic acid 1-cyano-6-nitro-3-phenyl-4, 7-nonadien-2-one (2R)-2-amino-2-mercapto-4-pentene MacBook Air F 44 F2 FS * & % $ 7 6 5 4 3 2 P Y T R E W Q O
L . CU311 2.11, 1120 38.26) Which of the following alkynes has the lowest boiling point? A) 3,3-dimethyl-1-butyne B) 1-hexyne C) 2-heptyne D) 3-hexyne E) 1-decyne 39.31) The carbon-carbon triple bond of an alkyne is composed of A) three o bonds B) three n bonds C) two o bonds and one t bond D) one o bond and two it bonds 40.65) When 2,2-dibromobutane is heated at 150°C in the presence of molten KOH, what is the major organic product?...