Question

Draw the reaction mechanism for the synthesis of methyl diantilis from 3-ethoxy-4-hydroxybenzaldehyde. Use NaOH/NaBH4 to produce...

Draw the reaction mechanism for the synthesis of methyl diantilis from 3-ethoxy-4-hydroxybenzaldehyde. Use NaOH/NaBH4 to produce 3-ethoxy-4-hydroxybenzyl alcohol first. Then use Amberlyst-15/1-propanol to produce the methyl diantilis. Include the mechanism for the reduction of NaBH4.

Science   Chemistry   
0 0
Add a commentTranscribed image text
Next >

Homework Answers

Answer #1

0 0
Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Log In

Sign Up

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Draw and explain the mechanism for the synthesis of dimethylmaleate (using Maleic anhydride, methyl alcohol and...
Draw and explain the mechanism for the synthesis of dimethylmaleate (using Maleic anhydride, methyl alcohol and sulfuric acid as the catalyst). Draw and explain the reaction mechanism for halogen-catalyzed cis-trans isomerization of dimethylmaleate.
Aldehydes can be reduced to primary alcohols by the strong reducing agent sodium borohydride, NaBH4(s). Draw...
Aldehydes can be reduced to primary alcohols by the strong reducing agent sodium borohydride, NaBH4(s). Draw the aldehyde, including all hydrogen atoms, you would use to produce each of the following primary alcohols: 2-methyl-1-propanol
Please draw the detailed reaction mechanism for the synthesis of epoxycyclohexane from cyclohexene
Please draw the detailed reaction mechanism for the synthesis of epoxycyclohexane from cyclohexene
(4) Draw the three elimination products formed by reaction of 2-bromo-4-methyl pentane with potassium tert-butoxide in...
(4) Draw the three elimination products formed by reaction of 2-bromo-4-methyl pentane with potassium tert-butoxide in 2-methyl-2-propanol. Circle the major product. Does this reaction follow Zaitsev’s or Hofmann’s rule?
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.
For Reduction of Vanillin aldehyde to Vanillyl alcohol using Nabh4, Aqueous NaOH and HCl If you...
For Reduction of Vanillin aldehyde to Vanillyl alcohol using Nabh4, Aqueous NaOH and HCl If you incorrectly add acid and do not attain a pH of 1, your yield may be lower than it should be as some of your product would not be isolated. Why won’t it be isolated? Notes: This addition of HCl causes four reactions to occur: a. it hydrolyzes the O-B bond in the intermediate and protonates the oxygen atom that was originally the oxygen atom...
26) Suggest a stepwise synthesis for 5-methyl-2-hexanone from 3-methyl-1-bromobutane. Using the reagents below, list in order...
26) Suggest a stepwise synthesis for 5-methyl-2-hexanone from 3-methyl-1-bromobutane. Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis. a. H2O / H2SO4, HgSO4 b. HC≡CNa c. 1. 9-BBN; 2. H2O2 / NaOH / H2O d. CrO3 / H2SO4 / H2O
Wittig Reaction:  synthesis an alkene ( olefin) from the reaction of an aldehyde or a ketone with...
Wittig Reaction:  synthesis an alkene ( olefin) from the reaction of an aldehyde or a ketone with a phosphorous ylide ( phosphorane ). The ylide is produced from phoshonium salt with a base ( NaOH ). The alkene synthesized is trans-9-(2-phenylethenyl)anthracene. 1.) The final product is an E isomer, although a Z isomer could potentially be formed. What is the definition of E and/or Z isomer of alkenes? How the group priority is established? 2.) Speculate why the E isomer is...
Performing Part II Multi-step synthesis part II: Fisher Esterification of m-nitrobenzoic acid to produce methyl m-nitrobenzoate...
Performing Part II Multi-step synthesis part II: Fisher Esterification of m-nitrobenzoic acid to produce methyl m-nitrobenzoate 1.) Which carbonyl compounds belong to class I carbonyl compounds and which carbonyl compounds belong to class II compounds? What is the characteristic reaction mechanism for each of the carbonyl class compounds? 2.) What is fisher esterification?
give a reaction mechanism for the following 1-4 and major product of 5 1. reaction of...
give a reaction mechanism for the following 1-4 and major product of 5 1. reaction of pentanol and phosphorus tribromide --> 1-bromopentane 2. reaction of sodium ethoxide and ethyl iodide --> diethyl ether 3. reaction of 3-methylhexanol and methane sulfonyl chloride --> 1-chloro-3-methylhexane 4. reaction of dehydration of propanol with sulfuric acid --> dipropyl ether 5. hexanol and HCL -->
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT