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- Question 4 a) Draw the two chair conformations of cis-1-chloro-2-methylcyclohexane a) Which is more stable, and by how much?Members of this series are not as chemcially reactive as the other hydrocarbons, and each has a higher molecular weight as a result of an additional -CH_2_. (That's suppose to be a small two) A) hydrocarbon B) polymer C) alcohol D) paraffin Can you help me understand which one it is please?!Draw the line bond structures for the following alkenes, cyclic alkenes, and alkynes: Can you explain to me about this part A) noncyclic alkenes that contain 4 carbon atoms (3 possible), please? Can you explain to me about this part B) cyclic alkenes that contain 4 carbon atoms (4 possible), please? Can you explain to me about this part C) alkynes that contain 4 carbon atoms (2 possible, neither of them is a cyclic alkyne), please?
- Question 3 CH3 a) Draw the chair conformations of the four cis-trans isomers of menthol (see structure on the right) b) Which is the most stable conformation? Explain your OH, answer. H3C CH33) Draw a cyclohexane chair with 3 substituents in the most stable conformation. Explain why the conformation you've chosen is the most stable.HO₂ H COOH COOH V POH HOT COOH cooff VI Ho HO COOH COOH VI H H COOH COOH VIIL OH OH Question: In the structures / examples abovke Identify V, VI, VII and VIII as Identical enantiomers, ciastereomes, stereo/cumers and/or structural isomers (there are 6 pairs 7 Comp eand to discover te I&T I TEN TEM TIMIN).
- Question 3 of 22 O Macmillan Learning > Organic Chemistry Maxwell Select the correct IUPAC name for the cycloalkane: F. Br The IUPAC name is: O 1-bromo-3-fluoro-6-propylcyclohexane 2-bromo-4-fluoro-1-propylcyclohexane O 3-bromo-1-fluoro-4-propylcyclohexane 1-propyl-2-bromo-4-fluorocyclohexane presented by Macmillan LearningCI ÓH a) Give the correct IUPAC name for the molecule above b) Draw a complete line-bond structure for the molecule. Include all lone pairs. c) Draw an isomer of the given molecule that is an ether (skeletal or full). d) Draw any correct stereoisomer of the given molecule e) Draw a diaesteromer of the molecule you drew in part d)Give the systematic name of the alkene, indicating cis or trans configuration. .CH3 H. CH3 systematic name: Draw trans-2-hexene. Include all hydrogen atoms. Select Draw Rings More Erase H
- Question s9 Explain why cyclohexane has less ring strain than cyclopropane.On the following energy diagram, identify the energy level of the cyclohexane conformation shown in the box. Energy (kJ/mol) A) I B) II CLU ||| IV Conformations 21. Answer the following: a) What is the IUPAC name of the acyclic unbranched alkane that contains six carbons? b) How are structural isomers best defined? i. compounds with the same molecular formula whose atoms are bonded together in different arrangements ii. compounds with the same molecular formula whose atoms are bonded together in the same arrangement, but drawn differently iii. compounds with similar structural formulas, but different numbers of hydrogens iv. none of the above c) Which of the following statements is false concerning line structures of alkanes? i. Each carbon atom has 4 bonds, although they may not all be shown explicitly ii. The lines represent bonds between the carbon atoms. iii. Hydrogen atoms are not shown because they are not present in the molecule iv. none of the above