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i)Draw bond-line structures for each of the following: [4 marks] a) 2-butyloxiraneo ZWn c) 2-methyl-3-hekyn-2-ol b)...
1. Draw line-angle structures for the following compounds: a) (20,4E)-1-chloro-3-methyl-2,4-hexadiene b) (32,5E)-4-methyl-3,5-nonadiene c) (32,5Z)-4,5-dimethyl-3,5-nonadiene d) (35,5E)-2,5-dibromo-3,5-octadiene
1. Draw the structures of the following compounds: a. 3-ethyl-4-methyl-2-hexene b.2-chloro-butyl acetate c. Ethylbenzene d. 2-methyl-3-pentanol e. 2-methylpropyl methyl ether 2. A) Distinguish between photodissociation and photoionization B) Use energy requirements of these two processes to explain why photodissociation of oxygen is more important than photoionization of oxygen at altitudes below about 90 km.
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
1) Draw the structure for each named compound: a) (Z)-N-ethyl-3-bromo-2-isopropyl-5- b) propanoyl chloride methyl-2-hexenamide c) benzoic anhydride d) (R)-3-chloro-4-ethylhexanoic acid e) ethyl 4-methylpentanoate f) pentanenitrile g) cyclohexanecarboxamide h) octyl butanoate 2) Provide an IUPAC name for each structure: b) 9 CH d) CH.CH нс снсон TH Page
2. Draw the bond-line formula for each of the following: a. Pentanoic acid: b. 2-bromo-3-methylhexanoic acid: c. 4-propylbenzoic acid:
2. Draw the bond-line structures of the following alkyl halides. Choose the compound that is mostly to undergo an S2 attack by a nucleophile in each of the following comparisons: a. chloromethane vs. 2-chloro-2-methylpropane (tert-butyl chloride) b. 2-chlorobutane vs. 1-chlorobutane c. l-chloro-2,2-dimethylpropane (neopentyl chloride) vs. l-chloropentane
Draw the structures of the following carbonyl compounds: 4-hydroxypentanoic acid ethyl ethanoate methyl 2-aminobenzoate 4-bromocyclohexanone 1-bromo-2-chloro-cyclopentane carboxylic acid
draw the structures of the following compunds:
1. Draw the structures of the following compounds: a. 3-ethyl-4-methyl-2-hexane 12V DAUI orgian antivollotor b.2-chloro-butyl acetate HDHO c. Ethylbenzene HOHO d. 2-methyl-3-pentanol HD HO-HD-HO-HO HD e. 2-methylpropyl methyl ether
ASAP PLEASE, THANKS!
Write a bond-line formula for each of the following compounds: a) trans-4-Isobutylcyclohexanol b) Neopentyl alcohol c) 4-Methyl-2-pentanol d) 2-Chlorohex-3-yn-1-ol
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections of the 2-3 bond in (2S,3R)-3-methylpentan-2-ol. [Marks: 2] (c) Based on the Newman projections from part b. - draw a rotation vs. energy diagram (you do NOT need to give specific energy values in this diagram) that will allow you to identify the most stable confirmation around the 2-3 bond. Assume the greatest steric and torsional strain occurs when the hydroxyl and ethyl groups...