draw the structures of the following compunds: 1. Draw the structures of the following compounds: a....
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.
PLEASE PROVIDE EXPLANATION 24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane 24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
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
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
30) Which of the following compounds is (are) symmetrical ethers? B)Only D) Only I, IIl, and IV A) Only III and IV C) Only I 31) What is the IUPAC of the following compound? но B) 1,1,4-Trimethyl-2-cyclohexanol D) 3,3,6-Trimethylcyclohexanol A) 2,5,5-Trimethylcyclohexanol ) 1,4,4-Trimethyl-2-cyclohexanol 32) What is the IUPAC of the following compound? он A) (R)-2,2-Dimethyl-3-pentanol C) (S)-2,2-Dimethyl-3-pentanol B) (S)-1-tert-Butyl-1-propanol D) (R)-4,4-Dimethyl-3-pentanol 33) What is the common name of the following compound? A) Methyl sec-butyl ether C) Isobutyl methyl ether B)...
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
Write structural formulas for the following compounds: a. 6-chloro-2,2-diiodo-3-heptyne b. toulene (methylbenzene) c. m-divinylbenzene d. 4-chloro-2-butyne e. 2-ethyl-3-methyl-1-pentanol f. ortho-dinitrobenzene
14. Which of the following reagents should be used to prepare tert-butyl ethyl ether a) tert-butyl bromide and sodium ethoxide b) tert-butyl alcohol and ethyl bromide c) tert-butyl alcohol and ethanol d) potassium tert-butoxide and ethyl bromide 15. What is the major organic product obtained from the following reaction? A) 1 B) 2 C) 3 D) 4 16. What product is formed when methyloxirane is treated with ethylmannesium bromide followed by treatment with aqueous acid? A) 1-pentanol B) 2-pentanol C)...
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)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.. T) for the compounds below, and use the cis/trans, R/S labeling when appropriate. E T D F 1a-Bromo-2-(trans) Chloro-4-(trans) Ethyl-3-(trans) Methyl-6-(Cis) 2-Hydroxypropyl-5-(trans)- (n-Propyl) Cyclohexane. Note, all of the groups orientations are in reference to la-Bromo Group all of the conformers specifications (e.g., axi the chair conformers of 1)- Give the correct names for the structures drawn (i.e. A-E)...