Question

1. predict the products of the reaction and show the mechanism if (W(O)6 is treated first...

1. predict the products of the reaction and show the mechanism if (W(O)6 is treated first with MeLi followed by Et3OBF4.

2. Draw the mechanism for the reaction of Ir(Cl)(CO)(PPh3)2 with methyl bromide.

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
1.) predict the products of the reaction between the following: 1-chloro-1-methyl cyclohexane and KOH in ethanol...
1.) predict the products of the reaction between the following: 1-chloro-1-methyl cyclohexane and KOH in ethanol Chlorocyclopentane and sodium ethoxide in methanol 2.) a 1.20g sample of cocaine [alpha]D=-16 was dissolved in 7.50 mL of chloroform and place in a polarimeter sample cell.( path length is 5 cm) What was the observed rotation? Show calculations 3.) draw the transition state structure of the E2 reaction between menthyl chloride and sodium and ethoxide
   1. Show all the products obtained from the ozonolysis of the following alkenes. a.     1-hexene...
   1. Show all the products obtained from the ozonolysis of the following alkenes. a.     1-hexene b.         2-methyl-2-pentene c.         cis-3-methyl-3-hexene d.         2,3-dimethylbut-2-ene e.        2,3-dimethylpent-2-ene 2. Stating whether the reaction between (+)-3-iodo-3-methylheptane and sodium ethoxide would follow SN1 or SN2 substitution mechanism, show the complete mechanism of the reaction emphasizing stereochemical changes observed, if any. 3. Showing the detailed stereochemistry, give the mechanism and products of epoxidation (with m-CPBA) and borane (with BH3-THF) addition reactions on cis- and...
The following mechanism has been proposed for the gas-phase reaction of chloroform (CHCl3) and chlorine. Cl2...
The following mechanism has been proposed for the gas-phase reaction of chloroform (CHCl3) and chlorine. Cl2 ? 2Cl (fast, reversible) Cl + CHCl3 ? HCl + CCl3 (slow) Cl + CCl3 ? CCl4 (fast) What rate law does this mechanism predict? (Choose from the list below and enter your answers in alphabetical order, e.g. ABC ). A)k G) [HCl]1/2 M) [Cl]2 B) [HCl] H) [Cl2]1/2 N) [CHCl3]2 C) [Cl2] I) [Cl]1/2 O) [CCl3]2 D) [Cl] J) [CHCl3]1/2 P) [HCl]2 E)...
Predict the products for the reaction of 2-phenylethanal with: 1.) Tollen's Reagent 2.) CrO3/H2SO4 3.) Cold...
Predict the products for the reaction of 2-phenylethanal with: 1.) Tollen's Reagent 2.) CrO3/H2SO4 3.) Cold Dilute potassium/H+/Heat 4.) Lithium aluminum hydride 5.) Sodium borohydride 6.) Phenylmagnesium bromide then water 7.) Cyanide in the presence of acid 8.) Hydoxylamine 9.) Phenylhydrazine 10.) 2,4-nitrophenylhydrazine 11.) Ethanol and dry HCl 12.) Semicarbazide
1. a. Explain why addition of HCl to 1, 2-dimethylcyclohexene yields a mixture of two products....
1. a. Explain why addition of HCl to 1, 2-dimethylcyclohexene yields a mixture of two products. b. Draw a mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide.
give SN1 or SN2 mechanism to each of the reactions: 1. methyl dalides react with sodium...
give SN1 or SN2 mechanism to each of the reactions: 1. methyl dalides react with sodium ethoxide in ethanol only by this mechanism 2. unhindered primary halides react with sodium ethoxide in ethanol mainly by this mechanism 3. the substitution product obtaind by solvolysis of tert-butyl bromide in ethanol arises by this mechanism 4. reactions proceeding by this mechanism are stereospecific 5. reactions proceeding by this mechanism involve carbocation intermediates 6. this mechanism is most likely to have been involved...
1. Draw the reaction mechanism for the formation of Grignard product From : Benzaldehyde to  Diphenylmethanol 2.Calculate...
1. Draw the reaction mechanism for the formation of Grignard product From : Benzaldehyde to  Diphenylmethanol 2.Calculate the theoretical yield for the reaction. Show your calculations. 3. Calculate the % yield of the reaction and the % error of the melting point. Show the calculations. 4. Locate an IR spectrum for the product in the literature 5. NMR analysis: Draw the full structure of the product. Show all bonds to the hydrogens. Label the different sets of hydrogens (i.e. Ha. Hb,...
draw the intermediate allyl cations and the products for the reaction of 1 equivalent of HCL...
draw the intermediate allyl cations and the products for the reaction of 1 equivalent of HCL to 2-methyl-1,3 butadiene. Identify the kinetic product and the thermodynamic product. What product predominates at low temperatures?
1) Draw the arrow pushing mechanism for the bromination of cyclohexene. 2) If this reaction was...
1) Draw the arrow pushing mechanism for the bromination of cyclohexene. 2) If this reaction was done using Br2in DCM, what product would you expect (show stereochemistry)?
Two stereoisomers are obtained from the reaction of HBr with (3S,4S)-4-bromo-3-methyl-1-pentene.1 Propose a mechanism for the...
Two stereoisomers are obtained from the reaction of HBr with (3S,4S)-4-bromo-3-methyl-1-pentene.1 Propose a mechanism for the reaction(provide a three-dimentional representation of the intermediates).Draw the structure of the two stereoisomers that form,showing stereochemistry of the new chiral centre.2. one of the stereoisomers is optically inactive.circle the optically inactive compound and explain why it is optically inactive.
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT