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- Draw two possible chair confirmations of cis-1-sec-butyl-4-chlorocyclohexanedraw (s)-4-ethyloctane in a structural condensed format. use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable Please provide only typed answer solution no handwritten solution needed allowedThe following cyclohexane derivative has three substituents-red, green, and blue. Identify each substituent as axial or equatorial, and identify each pair of relationships (red-blue, red-green, and blue- green) as cis or trans.
- Draw (S)-3-methyl he and in a structural condensed format. Use a dash or wedge bond to indicate stereochemistry of substitúyenos on asymmetric centers, where applicable.Draw (R)-4-ethyloctane in a structural condensed format. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.consider rotations about the C2-C3 bond of 3-methylpentane. draw the newman projection of any two energetically different eclipsed conformations, two energetically different staggered conformations. identify one conformation with both torsional and steric strain and another with only steric strain. identify the highest and lowest energy. please answer fast i give you upvote.
- Indicate what to do to obtain the compund (cyclohexylidenemethyl)cyclohexane from (C6H5)3P=CHCH2CH3(please don't use hend raiting and correct answer) Draw 5,5-bis(hydroxymethyl)-2-phenyl-13-dioxane in it's most stable chair conformation and circle all axial hydrogens.Q/choose the correct answer compounds which have equivalent bonds are: 1-organic comp. 2-saturated hydro carbon comp. 3-isomers 4-hybridization 5-free radical reaction
- Rank the following groups in order of decreasing priority. −H, −CH3, −Cl, −CH2ClDraw Newman projection: a) for the least stable conformation of 3- Methylbutane, view 2-3 bondb) The conformation with 2 Gauche interactions of 2-methylbutane view 2-3 bondA trisubstituted cyclohexane with three substituents-red, green, and blue-undergoes a ring-flip to its alternate chair conformation. Identify each substituent as axial or equatorial, and show the positions occupied by the three substituents in the ring-flipped form.