Draw the more stable chair conformation of the following molecules, and esti- mate the amount of...

Draw the more stable chair conformation of the following molecules, and esti- mate the amount of strain in each:

(a) trans-1-Chloro-3-methylcyclohexane

(b) cis-1-Ethyl-2-methylcyclohexane

(c) cis-1-Bromo-4-ethylcyclohexane (d) cis-1-tert-Butyl-4-ethylcyclohexane

Expert Solution

queen_honey_blossom answered 8 months ago

In Newman Projection, Draw the least stable conformation of propane. Then draw the most stable conformation...

In Newman Projection, Draw the least stable conformation of propane. Then draw the most stable conformation of propane

Draw both cis- and trans-1,4-dimethylcyclohexane in their more stable chair conformations

Draw both cis- and trans-1,4-dimethylcyclohexane in their more stable chair conformations. (a) How many stereoisomers are there of cis-1,4-dimethylcyclohexane, and how many of trans-1,4-dimethylcyclohexane? (b) Are any of the structures chiral? (c) What are the stereochemical relationships among the various stereoisomers of 1,4-dimethylcyclohexane?

A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead)...

A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead) representation, using wedges and hashed bonds to indicate the substituent positions. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). Be sure that both wedges/hashed bonds are drawn on the outside of the ring, or else the stereochemistry may be interpreted as square planar.

Given cyclohexane in a chair conformation, substitute two of the H labels with methyl and tert-butyl...

Given cyclohexane in a chair conformation, substitute two of the H labels with methyl and tert-butyl to construct the more stable conformation of trans-1-tert-butyl-3-methylcyclohexane. Use the numbering provided on the ring. Given cyclohexane in a chair conformation, substitute two of the H labels with methyl and tert-butyl to construct the more stable conformation of trans-1-tert-butyl-3-methylcyclohexane. Use the numbering provided on the ring.

Write the most stable Lewis structure (following formal charge rules) for the following molecules. (a) SOCl2...

Write the most stable Lewis structure (following formal charge rules) for the following molecules. (a) SOCl2 [Hint: Sulfur is the central atom.] (b) C2N2 [Hint: The two carbon atoms are connected in the middle of a chain.]

Using Newman Projection, draw the eclipsed and gauche conformation of the following compounds. 1. propane (C1-C2)...

Using Newman Projection, draw the eclipsed and gauche conformation of the following compounds. 1. propane (C1-C2) CH3CH2CH3 2. butane (C2-C3) CH3CH2CH2CH3 Why are both of the conformational isomers with a 0o and 120o dihedral angles considered to be in an eclipsed conformation?

12. a) Consider a sample of hemoglobin molecules all bound to carbon monoxide CO. What conformation...

12. a) Consider a sample of hemoglobin molecules all bound to carbon monoxide CO. What conformation would be favored? What would the Hill plot of that sample look like? b Consider a sample of hemoglobin molecules all bound to BPG. What conformation would be favored? What would the Hill plot of that sample look like?

Draw a Lewis structure for each of the following molecules and ions. In each case the...

Draw a Lewis structure for each of the following molecules and ions. In each case the ions can only be corrected in one way. (a) Br2 (b) H2S (c) N2H4

Consider 2-methylpentane, (CH3)2CHCH2CH2CH3 (analyzing the C3-C4 bond): Draw a Newman projection for the Gauche conformation. Draw...

Consider 2-methylpentane, (CH3)2CHCH2CH2CH3 (analyzing the C3-C4 bond): Draw a Newman projection for the Gauche conformation. Draw a Newman projection for the Anti conformation. Draw the Newman projection for the highest energy conformation of the C3-C4 bond of 2-methylpentane.

1) Draw and explain why the conformation freedom of peptides is limited. 2) Discuss the roles...

1) Draw and explain why the conformation freedom of peptides is limited. 2) Discuss the roles of hemoglobin and myoglobin in transporting oxygen and carbon dioxide

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