Question

What kind of reaction is involved in the derivative making mechanism of 1-Naphthylurethane from 3-methyl-1-butanol. Also...

What kind of reaction is involved in the derivative making mechanism of 1-Naphthylurethane from 3-methyl-1-butanol. Also what is the name of the derivative formed?

Homework Answers

Answer #1

1-Naphthylurethane is generally prepared by reacting isocyanates with alcohols. here, Isocyanates are electrophiles, and they are reactive toward a variety of nucleophiles (i.e. alcohols, amines, and water).

Upon treatment with an alcohol, an isocyanate forms a urethane linkage.

If we react 3-methyl-1-butanol with 1-Napthyl isocyante gives Isopentyl naphthalen-1-ylcarbamate (as derivative)

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
Consider the synthesis of tert-amyl chloride (2-chloro-2-methylbutane) from 2-methyl-2-butanol and HCl which has SN1 reaction. Explain...
Consider the synthesis of tert-amyl chloride (2-chloro-2-methylbutane) from 2-methyl-2-butanol and HCl which has SN1 reaction. Explain if a SN1 reaction would occur if the following(below) was changed. If an SN1 does occur, then state the IUPAC name of the product formed and compare the rate of reaction to the rate of the original reaction . In the event that SN1 does not occur, state the type of reaction that may occur and draw all the major products that could be...
Given 3.0 mL of 3-methyl-1-butanol how would I synthesize the derivative Naphthylurethane. Please provide a detailed...
Given 3.0 mL of 3-methyl-1-butanol how would I synthesize the derivative Naphthylurethane. Please provide a detailed procedure including techniques and amount of reagent needed for each step. Please note that this is a liquid alcohol and if possible use the smallest amount of alcohol needed. Please also include a reaction. Thank you. Also make sure to incoporate common laboratory reagents. Thank you.
What is the ph of 1-butanol, 2- butanol, and 2 methyl 2 propanol
What is the ph of 1-butanol, 2- butanol, and 2 methyl 2 propanol
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.
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.
What is the condensed structural formula of each compound named below? 3-ethylhexanal 2-methyl-3-heptanone 1,3-pentanediol 3-phenyl-1-butanol
What is the condensed structural formula of each compound named below? 3-ethylhexanal 2-methyl-3-heptanone 1,3-pentanediol 3-phenyl-1-butanol
In this experiment we synthesized t-pentyl chloride from 2-methyl-2-butanol using 12.0 M HCl and a sodium...
In this experiment we synthesized t-pentyl chloride from 2-methyl-2-butanol using 12.0 M HCl and a sodium bicarbonate wash. What effect would using an excess of 12.0 M HCl have on the rate of the reaction? Explain your answer.
How polar/what kind of a mobile phase is n-butanol, acetic acid, water in a 3:1:1 ratio...
How polar/what kind of a mobile phase is n-butanol, acetic acid, water in a 3:1:1 ratio for a TLC plate with silica gel? I am having a hard time understanding the interactions between stationary and mobile phases. Please help!
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...
Hydrolysis of; 3-methyl-4-cyclohexene-1,2-dicarboxylic anhydride to form a diacid. 1) Could someone please show me the reaction...
Hydrolysis of; 3-methyl-4-cyclohexene-1,2-dicarboxylic anhydride to form a diacid. 1) Could someone please show me the reaction mechanism of Maleic Anhydride, picric acid and piperylene. 2) If you can please also include FMOs and correlation diagrams. 3) Would you know which isomer if piperylene would be more reactive? Trans or Cis? Thankyou.
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT