Reaction of (15,2R,5R)-1-bromo-1,2,5-trimethylcyclohexane with t-butanol.
Draw the structure of (2R,5R)-2-bromo-5-methylheptanal.
Draw the reaction mechanisms for the Lucas test on ethanol, sec-butanol, and t-butanol with Lucas’s reagent (zinc chloride in concentrated HCl). Draw the reaction mechanisms for the Sodium test on ethanol, sec-butanol, and t-butanol.
4. (2 pts) Treating 3-methyl-2-butanol (see the following reaction) yields 2-bromo-2-methylbutane as the sole product. Propose a mechanism that explains the course of the reaction. (Recall: 1,2 shift of H) HBr OH
Question 2 4 pts Which is the bond-line structure for (15,2R)-1-bromo-2-chlorocyclohexane? ор
6-bromo-3-methyl-1-octanal Submit Ansr Incorrect. Tries 2/3 Previous Tries Br 4-bromo-1-butanol You are correct. our receipt no. is 156-1001Preious Tries Cl Cl 0 2,2-dichlorohexanoic acid You are correct. Your receipt no. is 156-9744 PreviousTries Submit Answr Tries 0/3 This discussion is closed Send Feedback
Draw the product formed by the reaction of potassium t-butoxide
with (1S,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw
the correct stereoisomer of the product.)
Draw the product formed by the reaction of potassium t-butoxide with (1S,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.)
Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. Reactant (2-methyl-2-butene) Reagent 1rightarrow Step 1 Product Reagent 2 rightarrow Step 2 Product Reagent 3 rightarrow Final Product (3-bromo-3- methyl-2- butanol)
4. Consider the compound (2R,3S)-2-bromo-1,1,3-trimethylcyclohexane. A. Will this compound undergo E2 reaction? Explain. Show relevant structures that justify your explanations to get full credit. B. Consider the following reaction: H-Br. 0. Draw the mechanism of the reaction to predict all the possible stereochemical products of the reaction. Show all electron flows using the curved arrows. (ii). Does the reaction produce a meso compound? Explain. Justify with relevant structures to get full credit. I
2 chloro butane reaction with silver nitrite 2 bromo butane reaction with silver nitrite 1 bromo butane reaction with silver nitrite 2 chloro 2 methyl reaction with silver nitrite 1 bromocycloheane reaction with silver nitrite write out reactions for each please
Which of these alcohols has the fastest reaction with HC1? 1-butanol 2-butanol tert-butyl alcohol