draw structures for the following compounds
1. 3-hexene
2. 2-pentyne
3. trans-3-hexene
4. cyclobutane
5. 3-ethyl-1-methylcyclohexene
3-hexene
2-pentyne
trans-3-hexene
cyclobutane
3-ethyl-1-methylcyclohexene
draw structures for the following compounds 1. 3-hexene 2. 2-pentyne 3. trans-3-hexene 4. cyclobutane 5. 3-ethyl-1-methylcyclohexene
draw the structures 2-Ethyl1,4-dimethylcycloheptane Cis-1,3-diethyl cyclobutane Trans-1-bromo-3-ethylcyclopentane Cis-1,2-diethyl cyclopropane Trans-1,2-diethyl cyclopropane 2-methylheptane 4-ethyl-2,2-dimethylhexane 4-ethyl-3,4-dimethyloctane 2,4,4-trimethylheptane 3,3-diethyl-2,5-dimethylnonane 4-isopropyl-3-methylheptane
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
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.
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42)-2,4-diethyl-1,4-hexadiene f) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5-tetramethyl-3-hexene i) Methylenecyclohexane, j) trans- 1,2 divinylcyclohexane
2. Which of the following compounds exhibit cis/trans Isomer CIS and transforms of the compounds that do exhibit Isomers s exhibit cis/trans isomerism? Explain why. Draw the a) Methylcyclobutane b) 3-ethyl-3-hexene c) 1-ethyl-3-methylcyclopentane d) 2,3-dimethylpentane e) 2,3-dichloro-2-hexene f) 2-butyne
Give an IUPAC name for the following compound: (E)-4-ethyl-3-methyl-2-hexene (E)-3-ethyl-4-methyl-2-heptene (Z)-3-ethyl-5-methyl-2-heptene (Z)-3-ethyl-4-methyl-2-heptene (E)-3-ethyl-4-methyl-2-hexene (E)-3-ethyl-5-methyl-2-heptene (2)-4-ethyl-3-methyl-2-hexene (2)-3-ethyl-4-methyl-2-hexene (Z)-3-ethyl-5-methyl-3-heptene (E)-3-ethyl-5-methyl-3-heptene
Name the product of the following reaction. cis-3-Hexene. trans-3-Hexene. 1-Hexene. trans-2-Hexene. cis-2-Hexene. Addition of 2 mol of HCl to 1-butyne would yield: CH_3CH_2CH_2CHCl_2 CH_3CH_2CCI_2CH_3 CH_3CH_2CHCICH_2Cl CH_3CH_2CH=CHCI CH_3CHCICHCICH_3 In the presence of excess hydrogen bromide, what is the major product of the addition of HBr to acetylene? 1, 3-dibromoethane 1-bromoethane 1, 1-dibromoethane 1, 2-dibromoethane 2-bromoethane Which of the following compounds is the major product when 1-hexyne is treated with excess HBr? 1, 1-dibromohexane 1, 1-dibromohexene 1, 2-dibromohexene 1, 2-dibromohexane 2, 2-dibromohexane
Draw clear, unambiguous skeletal structures of the kind drawn above) for each of the following compounds. 6-bromo-2,3-dimethyl-2-hexene 4,4-dimethyl-1-pentyne
Please provide a structure for each of the following names. 1-Bromo-3-methylcyclohexene 3-Ethyl-2-pentene cis-3-Octene (Z)-3-Methyl-2-hexene Vinylcycloheptane (Z)-1,3,5-Tribromo-2-pentene 1,2-Diethyl-cyclopentene Vinybromide 2,3-Dimethyl-2-butene 3,7,7-Trimethyl-4-octene 4-lsopropyl-1-nonene (E)-3-Methyl-2-heptene
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and an alkyl halide. f. Synthesize trans-2-hexene from 1-pentyne and an alkyl halide. Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.