Organic Chemistry 8th Edition solutions

Organic Chemistry 8
How could the following compounds be synthesized from acetylene?

Organic Chemistry 8
What is the major product obtained from the reaction of each of the following compounds with excess HCl? CH3CH2C CH CH3CH2C a. b. CCH2CH3 c. CH3CH2C CCH2CH2CH3

Organic Chemistry 8
Draw a condensed structure for each of the following: a. 2-hexyne e. methoxyethyne i. diethylacetylene b. 5-ethyl-3-octyne f. sec-butyl-tert-butylacetylene j. di-tert-butylacetylene c. methylacetylene g. 1-bromo-1-pentyne k. cyclopentylacetylene d. vinylacetylene h. 5-methyl-2-cyclohexenol l. 5,6-dim

Organic Chemistry 8
A student was given the structural formulas of several compounds and was asked to give them systematic names. How many did she name correctly? Correct those that are misnamed. a. 4-ethyl-2-pentyne b. 1-bromo-4-heptyne c. 2-methyl-3-hexyne d. 3-pentyne

Organic Chemistry 8
Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw curved arrows to illustrate the bond-making and bond- breaking processes.

Organic Chemistry 8
What is each compounds systematic name?

Organic Chemistry 8
What reagents should be used to carry out the following syntheses?

Organic Chemistry 8
a. Draw the structures and give the common and systematic names for alkynes with molecular formula C7H12. Ignore stereosiomers. (Hint: There are 14.) b. How many would there be if stereoisomers are included?

Organic Chemistry 8
Draw the mechanism for the following reaction:

Organic Chemistry 8
How can the following compounds be synthesized, starting with a hydrocarbon that has the same number of carbons as the desired product? a. O CH3CH2CH2CH2CH b. CH3CH2CH2CH2OH c. O CH3CH2CH2CCH2CH2CH2CH3

Organic Chemistry 8
What reagents would you use for the following syntheses? a. (Z)-3-hexene from 3-hexyne b. (E)-3-hexene from 3-hexyne c. hexane from 3-hexyne

Organic Chemistry 8
What is the major product of the reaction of 1 mol of propyne with each of the following reagents? a. HBr (1 mol) e. aqueous H2SO4, HgSO4 h. H2/Lindlar catalyst b. HBr (2 mol) f. R2BH in THF followed by i. sodium amide c. Br2 (1 mol)/CH2Cl2 H2O2/HO- /H2O j. the product of part i followed by d. Br2 (2

Organic Chemistry 8
Answer Problem 39, parts ah, using 2-butyne as the starting material instead of propyne.

Organic Chemistry 8
What is each compounds systematic name?

Organic Chemistry 8
What is the molecular formula of a hydrocarbon that has 1 triple bond, 2 double bonds, 1 ring, and 32 carbons?