Chapter 3: 39P (page 189)
Give the IUPAC name of the following alkanes.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
Short Answer
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
Chapter 3: 39P (page 189)
Give the IUPAC name of the following alkanes.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
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Get started for freeProvide IUPAC names for the following compounds.
(a)
(b)
(c)
(d)
(e)
( f)
Draw the both chair conformations of each of the following substituted cyclohexanes. In each case, label the more stable conformation.
(a)
(b)
(c)
(d)
Table 3-6 shows that the axial-equatorial energy difference for methyl, ethyl, and isopropyl groups increases gradually: 7.6, 7.9 and 8.8 kJ/mol (1.8, 1.9, and 2.1 kcal/mol). The tert-butyl group jumps to an energy difference of 23 kJ/mol (5.4 kcal/mol), over twice the value for the isopropyl group. Draw pictures of the axial conformations of isopropylcyclohexane and tert-butylcyclohexane and explain why the tert-butyl substituent experiences such a large increase in axial energy over the isopropyl group.
Question: Conformational studies on ethane-1,2-diol (HOCH2 -CH2OHhave shown the most stable conformation about the central C-Cbond to be the gauche conformation, which is 9.6 KJ/mol (2.3 kcal/mol)more stable than the anti-conformation. Draw Newman projections of these conformers, and explain this curious result.
Question: Using the general formula for alkanes
(a) Predict the molecular formula of thestraight chain alkane.
(b) Predict the molecular formula of the alkanes containing 42 carbon atom with extensive branching.
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