3. Write a bond-line formula for each of the following compounds: (a) 1,4-Dichloropentane (b) sec-Butyl bromide...
I . Write a bond-line formula for each of the following compounds: 1,4-Dichloropentane sec-Butyl bromide 4-Ethyl-3,3-dimethylhexane 2,2,3-Trimethylpentane 3-Ethyl-2-methylhexane Bicyclo[4.4.0]decane 2,2-Dicyclobutyl-5-ethyloctane Bicyclo[2.2.1]heptane 4-Isopropyl-5-methyloctane cis-1-sec-Butyl-2-methylcyclopentane 3,7-Diethyl-2,2-dimethyl-4-isopropylnonane 4-Ethyl-4-fluoro-2-methylheptane 1,1-Dichlorocyclopentane cis-1,2-Dimethylcyclopropane trans-1,2-Dimethylcyclopropane II. Give systematic IUPAC names for each of the following: а. ОН b. С. Br d. e. Br f. Br Br CI h. а. ОН b. С. Br d. e. Br f. Br Br CI h.
8. Draw 3 of the following compounds: a. Tribromomethane b. 2,2-dicyclopropyl-3,3-dimethylbutane c. Di-(2,3-hydroxymethyl)-1,4-decandiol d. cis-2-propoxy-1-cyclodecanol 9. Draw the Newman projection for the following compounds: a. 13-dibromo-2,4-dichloropentane C,-C2 b. -fluoro-3-methoxy-4-methylethylheptan-2-ol C2-C
OCH3 3. Indicate the electrophilic or nucleophilic centers for the following compounds: a) b) d) 4. Answer the following questions regarding 2,3-dimethylbutane: a) draw any staggered Newman projection of this compound looking down the C2-C3 bond. b) draw the highest energy conformation (as a Newman projection). Label each example of steric and/or torsional strain. c) draw the lowest energy conformation. Identify any sources of steric or torsional strain if present. m md iminetahm 5 Draw tra possiblechair conformatex For Jbrom-s-7ethiTmethychayo...
Can you answer the questions given in the photos above? The sec-butyl cation can react as both a Lewis acid and a Brønsted- Lowry acid in the presence of a water-sulfuric acid mixture. In each case, however, the product is different. The two reactions are: 2. H2o +H3O+ a. In which reaction does this cation react as a Lewis acid? In which does it react as a Brønsted-Lowry acid? b. Write Lewis structures for reactants and products and show by...
1) 2-amino-3-hydroxybutanoic acid 2) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
1.) 2-amino-3-hydroxybutanoic acid 2.) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
can anyone do #3 Construct the molecular models for each of the following compounds and study their conformations, geometry, bond angles, hybridization and any other features. In your lab report, show the structures using bond-lines. For numbers 1, 2, and 9, write the IUPAC name for each molecular structure.obyo ls.0 1. all structural isomers of CsH14 to smoal. t 2. all structural isomers of CsH11Cl 3. all structural isomers of CaHs0 4. all structural isomers of C2H4, C2H2CI2, C2H2, C3H4,...
Problem 13. Write a bond-line formula for each of the following compounds. (a) (E)-1,4-dibromopent-2-ene (b) (R)-3-chloro-2-methylbut-l-ene Problem 14. You have the task of preparing styrene (C.HSCH=CH;) by dehydrohalogenation of either 1- bromo-2-phenylethane or 1-bromo-1-phenylethane using KOH in ethanol at reflux temperature. Which halide would you choose as your starting material to give the better yield of the alkene Explain your answer. Problem 15. The reactions below are unlikely to occur as described. Predict the true major product and the reaction...