Chapter 11: 8P (page 426)
Draw additional resonance structures for each cation
(a)
(b)
(c)
Short Answer
(a)
(b)
(c)

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Chapter 11: 8P (page 426)
Draw additional resonance structures for each cation
(a)
(b)
(c)
(a)
(b)
(c)

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Draw the organic products formed when each alkyne is treated with two equivalents of HBr.
a.
b.
c.
Which bases can deprotonate acetylene? The pKa values of the conjugate acids are given in parentheses.

What two enols are formed when pent-2-yne is treated with H2O, H2SO4 and , HgSO4? Draw the ketones formed from these enols after tautomerization.
Question: Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other organic and inorganic compounds. Then draw the synthesis in the synthetic direction, showing all needed reagents.
Give the IUPAC name for each compound.
a. 
b.
c. 
d.
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