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Organic Chemistry
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)
Draw the 3-dimensional structural formula for ® 2 -iodopentane. Use the wedge and dashed line convention.
Complete the table below based on whar you know about enantiomers.
Property d-menthol l-mentholMelting point 35 degrees CWater solubility 1.4g/100mLDensity 0.90 g/mLRotation of planePolarized light +48 degreesRotation of planePolarized light of d,l mixture
Circle the chiral carbons in d- menthol. Assign absolute ( R vs S) configuration for each of the carbons you have circled.
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
This assignment inhibits chemistry Laboratory Questions.
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