Textbook QuestionAuthentic skunk spray has become valuable for use in scent-masking products. Show how you would synthesize the major component of skunk spray 3-methylbutane-1-thiol from any of the readily available butene or from buta-1,3-diene.546views
Textbook QuestionMany hunting dogs enjoy standing nose-to-nose with a skunk while barking furiously, oblivious to the skunk spray directed toward them. One moderately effective way of lessening the amount of odor is to wash the dog in a bath containing dilute hydrogen peroxide, sodium bicarbonate, and some mild dish detergent. Use chemical reactions to describe how this mixture helps to remove the skunk spray from the dog. The two major components of skunk oil are 3-methylbutane-1-thiol and but-2-ene-1-thiol.370views
Textbook QuestionUsing an alkyl halide and a thiol as starting materials, how would you prepare the following thioethers? c. d. 454views
Textbook Question(•••) THINKING AHEAD Thiols are prone to dimerize through the formation of a disulfide bond in a reaction that stylists use to induce permanent curls in hair. [You'll learn about the importance of this reaction to protein structure in biochemistry.] What type of reagent would you use to effect this transformation?<IMAGE>337views
Textbook QuestionStarting with hydrogen sulfide, suggest a synthesis of the following thioether that makes use of two different haloalkanes.<IMAGE>333views
Textbook QuestionShow how you would synthesize butyl isopropyl sulfide using butan-1-ol, propan-2-ol, and any solvents and reagents you need.454views
Textbook QuestionThiols can be prepared from the reaction of thiourea with an alkyl halide, followed by hydroxide-ion-promoted hydrolysis. a. Propose a mechanism for the reaction.804views
Textbook Questionb. What thiol will be formed if the alkyl halide employed is pentyl bromide?405views
Textbook QuestionDithiothreitol reacts with disulfide bridges in the same way that 2-mercaptoethanol does. With dithiothreitol, however, the equilibrium lies much more to the right. Explain.<IMAGE>299views
Textbook QuestionUsing an alkyl halide and a thiol as starting materials, how would you prepare the following thioethers?a. <IMAGE>327views
Textbook QuestionUsing an alkyl halide and a thiol as starting materials, how would you prepare the following thioethers?b. <IMAGE>255views
Textbook Question(a) Show how you would synthesize the pure (R) enantiomer of 2-butyl methyl sulfide, starting with pure (R)-butan-2-ol and any reagents you need(b) Show how you would synthesize the pure (S) enantiomer of the product, still starting with (R)-butan-2-ol and any reagents you need.214views
Textbook QuestionShow how you would synthesize the following:(e) cis-pent-2-en-1-thiol from a suitable alkenyl halide242views
03:21
