1) Draw line-angle structures for these compounds.
a. cis-2-pentene b. 1-butanol c. butanone
2) Identify the strongest IMF for each of the above
compounds.
a. ____________________ b. __________________ c.
________________________
3) Draw at least 2 molecules of these compounds showing the IMFs
that form between them.
a. Cis-2-pentene (draw 2 or more molecules) b. 1-butanol (draw 2 or
more molecules)
4) Which of the three compounds in question 1 is the most soluble
in water? Give a brief explanation and draw that molecule showing
how it interacts with water molecules.
1) Draw line-angle structures for these compounds. a. cis-2-pentene b. 1-butanol c. butanone 2) Identify the...
Which of these three compounds are the most soluble in water? cis-2-pentene, 1- butanol or butanone? Give a brief explanation and draw that molecule showing how it interacts with water molecules.
1 11-15. Determine the relationship between the following pairs of compounds. 11 trans-2-pentene and cis-2-pentene A) structural isomers 12. trans-2-pentene and cyclopentane B) Enantiomers C) not related 13. hexane and 2-methybutane D) same molecule 14. trans-2-heptene and trans-2-hexene E) geometrical (cis/trans) isomers 15 glycerol and 1,2-ethandiol (stereoisomers)
1. Draw the following molecules using line structures. (20 points) (L.)4-methyl-1-pentene (2.) -1,2-dimethyl-cycloptutade 2. Determine the molecular formula for the following structurw. (20points) 3. The following molecule bes c arbon atoms in total and is an example of a (saturaledunsaturated fatty acid with _ſcis/trans) configuration. (15 points) 4. Draw the mirror Image of the following molecule. Then, determine if they are enantiomers or identical. Circle the chiral center if prosent (15 points) CHE 5. Circle and label the carboxylic acid...
Discussion Questions The structures of acetanilide and malonic acid are provided below 1. For each structure, draw circles around the polar and nonpolar regions of the molecule, and label each circled regiorn with the type of intermolecular attractive force it can use to interact with other molecules. Acetanilide Malonic Acid но CH2 OH 2. Now-thoroughly explain (on the basis of polarity/nonpolarity and intermolecular attractive forces) how the acetanilide was separated from the malonic acid by recrystallization from water. And explain...
Please and thank you. Problem 12.29 Draw the line-angle formula for 1-pentene. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advane 12D H2 H + C Cl Br I Previous Answers Request Answer Submit XIncorrect; Try Again; 4 attempts remaining z OS Part C Draw the condensed structural formula for 2-methyl-1-butene. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), A 12D Ht H Marvin JS S...
Identify the reagents for all three steps. Draw the structures of organic compounds A and B. Omit byproducts. Reagents given: - Mg - 1. ethylene oxide 2. H3O+ - PCC - 1. CH3CO3H 2. H2O - H2, Pt - 1. O3 2. Zn, H2O - 1. CH3MgBr 2. H3O+ - 1. O3 2. H2O2 Identify the reagents for all three steps. Draw the structures of organic compounds A and B. Omit byproducts.
6. Build the cyclobutane ring and study the angle strain and torsional strain. Draw the structures to explain these factors. 7. The conformation of cyclobutane is slightly folded. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. Compare this actual structure with the hypothetical planar structure. Draw the relevant structures. 8. trans-1,2-Dimethylcyclobutane is more stable than cis-1,2-dimethylcyclobutane, but cis-1,3- dimethylcyclobutane is more stable than trans-1,3-dimethylcyclobutane. Use the molecular models to find the reasons for...
Name or draw the following molecules (use cis/trans naming system) 1. Name or draw the following molecules (use cis/trans naming system): CI CI CH3 CH2CH3 a. b. c. 4-ethyl-6-(1,2-dimethylpropyl)decane 2. Draw all of the resonance structures for the following compounds. CH2
7. Conformational Analysis: Chairs (25 points) Consider the following compounds: trans-1-Fluoro-2-iodocyclohexane and cis-1-Fluoro-2-iodocyclohexane Draw the skeletal structures and two chair conformations of each. Chair templates are provided for the cis compound. Redraw your own chairs for the trans compound. Circle the more stable conformation of each compound and briefly explain your selections below each pair, including the specific types of steric strain involved. Short phrases are great complete sentences not required! trans-1-Fluoro- 2-iodocyclohexane explanation for more stable conformation: cis-1-Fluoro- 2-lodocyclohexane...
Can you show me the mechanism for 1-Butanol to Cis-2-Butene and trans-2-butene? (Does the carbocation shift from c1 to c2, then a hydride shift from c2 to c1 (kicking off the water), then another water molecule takes a hydrogen from c3, with the electrons then going from c3, to share between c3 and c2?) Many carbocation rearrangements involve hydride shifts (Section can also migrate to a positively charged carbon. in the direction that leads to a more stable carbocation. 5.12)...