Question



Which of the following amines can be prepared by ring opening of an epoxide with sodium amide followed by reduction? OH NH2 O
0 0
Add a comment Improve this question Transcribed image text
Request Professional Answer

Request Answer!

We need at least 10 more requests to produce the answer.

0 / 10 have requested this problem solution

The more requests, the faster the answer.

Request! (Login Required)


All students who have requested the answer will be notified once they are available.
Know the answer?
Add Answer to:
Which of the following amines can be prepared by ring opening of an epoxide with sodium...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Similar Homework Help Questions
  • 9. Which of the following amines can be prepared by ring opening of an epoxide with...

    9. Which of the following amines can be prepared by ring opening of an epoxide with sodium amide followed by reduction? CH OH Em Em a. only 1 b. only 1 and 2 c. only 1 and 4 d. 1, 2, 3 and 4 10. What is the IUPAC name of the following compound? OH HO. Y OH ÕH a. (2R 3R)-dihydroxybutanedioic acid b. (2S,3S)-dihydroxybutanedioic acid C. (2R,3S)-dihydroxybutanedioic acid d. (2S,3R)-dihydroxybutanedioic acid 11. Which of the following is the correct...

  • Worksheet for Epoxides & Amines redicted product needed for the following epoxide opening. Indicate stereochemistry. NaOH...

    Worksheet for Epoxides & Amines redicted product needed for the following epoxide opening. Indicate stereochemistry. NaOH a. b. 2. Wha t is the required starting material for this reaction? Indicate stereochemistry. 1. 2. H,O* 3. Draw the intermediate and expected product for the following reaction sequence. NH2 excess CH, Br NaOH, Δ H3 use CHsBr to convert amines to ammoniums for Hofmann elimination? Hint: think about what could happen if we use CHaCH2Br.

  • 2 1 attempts left Check my work Which of the following amines can be used to resolve a racemic mi...

    Please answer all questions. The answer to question #2 is incorrect. 2 1 attempts left Check my work Which of the following amines can be used to resolve a racemic mixture of amino acids? Select all that apply. 0.5 points NH2 HIH eBook Ho Print NH2 References Be sure to answer all parts. The structure of the amino acid sequence Gly-His-Leu is shown below. Select the letters that correspond to the N-terminal(s), the C-terminal(s), and amide bond(s). (CH3)2CHCH2 0.5 points...

  • Please answer all questions 13) Which of the following are intermediates in the acid hydrolysis of...

    Please answer all questions 13) Which of the following are intermediates in the acid hydrolysis of an amide? Hyo. he at NH, SOH но он HO, OH RANH NH RAH он RNH н н 2 4 A) 1 B) 2 C) 2 & 3 D) 4 E) 1, 2, & 3 14) Acids can be reduced to aldehydes by A) treatment with LiAlH4 B) conversion to the acid chloride followed by treatment with LiAlH[OC(CH3)313 C) conversion to the amide followed...

  • please help answer Question 1 and Question 2. thank you [2] QUESTION 1 Which of the...

    please help answer Question 1 and Question 2. thank you [2] QUESTION 1 Which of the following compounds have been assigned the correct IUPAC name? OH 1-Methyl-2-propyloxycyclohexane (2) 6-Methoxy-oct-3-enoic acid Br (3) Isopropyl 3-methylbutanoate 5-Bromo-4-methylhept-2-yne A All of the compounds (1) – (4) have been correctly named (2), (3) and (4) only - с (2) and (4) only D (1) and (3) only. QUESTION 2 [2] The following is a structure of methotrexate, a drug used to treat cancer, autoimmune...

  • When acyl halides (R?COX) or acid anhydrides (R?OC?O?CO?R) react with primary amines (R?NH2) or secondary amines...

    When acyl halides (R?COX) or acid anhydrides (R?OC?O?CO?R) react with primary amines (R?NH2) or secondary amines (R2NH), the reaction yields an amide: O   ||   R?C?NR2 where R may be an alkyl group or hydrogen atom. For example, propanoyl chloride (       O        ||CH3CH2C?Cl) reacts with ethanamine (CH3CH2NH2) to form (O         ||         CH3CH2C?NHCH2CH3). The IUPAC name for the product isN-ethyl propanamide, as it is formed from ethanamine and propanoyl chloride. Match the names of the products for the following reactions. Identify the products by dragging the appropriate labels...

  • Epoxides, like bromonium ions and mercuronium ions, can be ring-opened with various nucleophiles. The stereochemistry of...

    Epoxides, like bromonium ions and mercuronium ions, can be ring-opened with various nucleophiles. The stereochemistry of the product depends on if the ring-opening occurs under acidic or basic conditions. The following two reactions – ring opening of an epoxide with water – illustrate this effect. Explain why the outcome of the reaction changes under these two conditions and provide electron-pushing arrows to explain the mechanisms. PHOLD H30*/H20 PHOI OH | PhD NaOH,H,O HO D

  • uestion 2 Rank these molecules in order of decreasing acidity [that is, most acidic first.] 1. CHCHCO2Н 2....

    uestion 2 Rank these molecules in order of decreasing acidity [that is, most acidic first.] 1. CHCHCO2Н 2. CH-CHCO,н F 3. CH-CН-СО,Н 2 3 1 2> 1> 3 1> 2 3 3> 2 11 O 1>3> 2 Question 3 Which compound is the most acidic? Cl CI C Question 5 Which of the following molecules is the product of an aldol reaction? ОН HO HO IV ОН and IV Question 11 Which of the following contains an amide functional group?...

  • Amines can be made by the reduction of nitriles, which in turn can be made from...

    Amines can be made by the reduction of nitriles, which in turn can be made from an alkyl halide. Draw the structures of a starting alkyl bromide and the intermediate nitrile that would be used in the synthesis of 3-methylbutylamine (also known as isoamylamine). Do not show free ions. alkyl bromide nitrile isoamylamine NC 1.LAH 2.H,0 "NH2

  • I think the answer that we discussed in class for this problem was D but I...

    I think the answer that we discussed in class for this problem was D but I do not know why. What indications should I be looking at to determine that the pH range of these substances? NH HO (1) 2. A 0.0010 Maqueous solutions of each of the substances below was prepared. Which of these solutions will have a 8 s pHS 12? CHg N NH2 OH NH2 (25 (3) (5) A C2H₂O, Only (2) C3H, NO CuloN Cat₂0 B...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT