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    Bond Dissociation Energies and Yield

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    4. Use the bond dissociation energies (kcal/mole) listed below to predict which of the following statements 1 or 2) would be expected to yield the most product. Be sure to show your work.
    R-H (98) R-C (81) RI (53) Cl-Cl (58) I-I (36)
    H-Cl (103) H-I (71)

    1) RH (g) + Cl 2 (g) - > RCL(g) + HCL (g)
    2) RH (g) + I2 (g) -> RI (g) HI (g)

    6.Draw the 3-dimensional structural formula for ® 2 -iodopentane. Use the wedge and dashed line convention.
    7. b.Complete the table below based on what you know about enantiomers.

    Property d-menthol l-menthol
    Melting point 35 degrees C
    Water solubility 1.4g/100mL
    Density 0.90 g/mL
    Rotation of plane
    Polarized light +48 degrees
    Rotation of plane
    Polarized light of d,l mixture

    c.Circle the chiral carbons in d- menthol. Assign absolute ( R vs S) configuration for each of the carbons you have circled.

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    Solution Summary

    The yield of the organic products is determined by bond dissociation energies. Three dimensional structures for 2 -iodopentane is given. The enantiomers are given.

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