Draw bond-line structures for the following compounds. 1.) 6-tert-butyl-2,2,3,3-tetramethylnonane 2.)3-cyclohexyl-2,2,4-trimethylheptane 3.) 4-secbutyl-4,5-diisopropylnonane 4.)1,3-dicyclopentylcycloheptane
Draw bond line structures for the following: 1,1,3-triethylcyclooctane 4,5-diethylnonane 1-butyl-3-fluorocyclobutane 4-ethyl-3-isopropyl-2-methylhexane
Draw the Bond-Line structures for the following compounds. a) 1-Bromo-6-(2,2,3-trimethylbutyl) undecane b) (CH3)2CHCHC(CH3)2 c) 2,5-dicyclobutyl-4-ethylheptane d) 1-tert-butyl-3-fluorocyclohexane
Draw the structures for the following compounds: (3Z,5Z)-2-chloro-4,5-diethyl-3,5-nonadiene PLEASE EXPLAIN! (3 points) Draw the structures for the following compounds: (3Z,5Z)-2-chloro-4,5-diethyl-3,5-nonadiene . ZE
Name the first two and draw the last two Cl 2. Draw the following compounds 1,3-dibromo-4-methylheptane 6-butyl-1-iodo-3-methyldecane
How would you draw the most stable conformation of trans-1-tert-butyl-4-isopropylcyclohexane? Axial tert-butyl group on C-1, Axial isopropyl group on C-4 Axial tert-butyl group on C-1, Equatorial isopropyl group on C-4 Equatorial tert-butyl group on C-1, Axial isopropyl group on C-4 Equatorial tert-butyl group on C-1, Equatorial isopropyl group on C-4 Choices b and c are both correct Choices a and d are both correct تسليم الجواب Tries 0/1 How would you draw the most stable conformation of trans-1,3-cyclohexanediol? Axial hydroxyl...
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
3. Write a bond-line formula for each of the following compounds: (a) 1,4-Dichloropentane (b) sec-Butyl bromide (c) 4-Isopropylheptane (d) 22.3-Trimethylpentane (e) 3-Ethyl-2-methylhexane 6. Give systematic IUPAC names for each of the following: (b) X OH (c) 7. Sketch curves similar to the one given in Figure 3.9 showing the energy changes that arise from rotation about the C2-C3 bond of the two compounds below. You need not concern yourself with actual numeri values of the energy changes, but you should...
for each pair of compounds, state which is the better SN2 substrate 2-methyl-1-iodopropane or tert-butyl iodide 2-methyl-1-iodopropane O tert-butyl iodide Submit Request Answer Part B cyclohexyl bromide or 1-bromo-1-methylcyclohexane 1-bromo-1-methylcyclohexane cyclohexyl bromide 2-bromobutane or isopropyl bromide O isopropyl bromide 2-bromobutane Submit Request Answer Part D 1-chloro-2,2-dimethylbutane or 2-chlorobutane O 1-chloro-2,2-dimethylbutane 2-chlorobutane 1-iodobutane or 2-iodopropane O 2-iodopropane O 1-iodobutane Submit Request Answer
Draw the structures of the following organic compounds a) 2,4-dicholoroheptane b) 2,2-dicholorohexane c) 2-methyl-4-ethylnoname d) 2,2,4-trimethyldecane e) 2-methyl-3-isoprophylheptane f) 1-methylcyclohexane g) 1,1-diethylcyclopentane h) 1-bromo-2-methylcycloheptane i) 1,2-dichlorocyclobutane
7) Write the structures for the following compounds. Which of the compounds are unsaturated? a) 3,5,5-trimethylheptane d) 3-ethyl-5-methyloctane CHsCH2CHCH2 CCH3 b) 4-phenyl-2-hexyne e) 3,4-dibromo-2-pentene 0) 3,4- dichforo- 4-methyl-1-pentene f) 2,3,4-tribromohexane