Question

When should you use a protecting group, such as an acetal? A-When the most reactive functional group is not the one you want
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Protecting group such as an acetal is used when

B) When an alcohol is present in your molecule.

These protections replace the acidic proton on an alcohol

Add a comment
Know the answer?
Add Answer to:
When should you use a protecting group, such as an acetal? A-When the most reactive functional...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Protecting groups are used in synthesis when a starting material contains multiple reactive sites. This neutralizes...

    Protecting groups are used in synthesis when a starting material contains multiple reactive sites. This neutralizes one of the reactive sites and makes it inert to the reaction conditions. The protecting group can then be selectively removed to re-form the reactive site. Analyze the molecule below and answer the three questions. Identify the protecting group. Which reagent was used to install this protecting group? Which reagent is used to remove the protecting group? H3C CH3 Si CH3 CH3 CH3

  • Protecting groups are used in synthesis when a starting material contains multiple reactive sites. This neutralizes...

    Protecting groups are used in synthesis when a starting material contains multiple reactive sites. This neutralizes one of the reactive sites and makes it inert to the reaction conditions. The protecting group can then be selectively removed to re-form the reactive site. Analyze the molecule below and answer the three questions. H3 C CH3 SCH BV сна CHI ntify the protecting group. Which reagent was used to install this protecting group? Which reagent is used to remove the protecting group?...

  • IM HAVING DIFFICULTIES TO IDENTIFY NMR, can you please explain in details this answer and whats t...

    IM HAVING DIFFICULTIES TO IDENTIFY NMR, can you please explain in details this answer and whats the easiest way to read it The reaction is worked up and compared to the starting material by NMR Staring material (methyl (S 2-methy-4-cxobutanoate) Product зн 러 зн H 24 3H 2H 10 PPM 2 PPM Question #14: Does it appear that the correct product has formed? Examine your reasoning type your text here For example, if you had an alcohol and an aldehyde...

  • Please explain what is going on in this lab for STEP 3. what are some important...

    Please explain what is going on in this lab for STEP 3. what are some important factors? Multistep Synthesis Preparation of 4,4-Diphenyl-3-buten-2-one! This experiment illustrates se multistep synthesis, in which the the next. This process is very common iment illustrates several important concepts of organic synthesis. It is a synthesis, in which the product of one reaction becomes the starting material of This process is very common in industry and research, and demands careful to vields and techniques. The experiment...

  • Question 4 2 pts Use the following to answer the questions below: For each set of...

    Question 4 2 pts Use the following to answer the questions below: For each set of reactants, select a correct product characterization from the response list. Responses may be used more than once or need not be used at all. a) hemiacetal b) acetal c) alkene d) alcohol Ketone, two alcohols, acid catalyst Question 6 Use the following to answer the questions below: Characterize each compound in terms of functional groups present using the response list. Responses may be used...

  • QUESTION 1 Identify the functional group in the molecule below (there is only one). Spelling counts!...

    QUESTION 1 Identify the functional group in the molecule below (there is only one). Spelling counts! o CH3(CH)16COCH(CH)10CH3 QUESTION 4 Identify the functional group in the molecule below (there is only one). Spelling counts! O CH-CH-CH-CH-CH-CH-COH QUESTION 5 Give the IUPAC name of the molecule below. Use only lowercase letters (no capitals). Spelling and punctuation count! Your answer must match EXACTLY to be counted correct. Hint: work it out on scratch paper first. CH CH, CH,CH-C-CH.CHCHCHCH:CH, CH, CH.CH QUESTION Give...

  • Total Points:/36 Section 1: Multiple Choice (6 pts) AIkyl halides can be converted into Grignard reagents...

    Total Points:/36 Section 1: Multiple Choice (6 pts) AIkyl halides can be converted into Grignard reagents by which of the following methods? 1. a. Retluxing alky I halide and adding Mg metal in Alcohol solution. b. Reluxing with MgC solution c. Warming solution and adding Mg powder in dry Diethyl Ether. d. A and C, but not B. 2. In the Nylon experiment, why was NaOH added to the aqueous layer? Catalyze reaction Increase reaction rate Neutralize HCl as it...

  • 1) Choose one molecule from the set and create an 8-step synthesis scheme using the chosen...

    1) Choose one molecule from the set and create an 8-step synthesis scheme using the chosen molecule as your starting material. You need to write the complete set of reagents and draw the product expected from each step. Reagents typically used together are considered one step, eg. 1) LAH 2) H.O should be considered as one step Your 8 steps must include at least one reaction from each of the chapters, aldehydes and ketones, carboxylic acid derivatives, alcohols. You can...

  • fill in reaction table below. Make sure you correctly calculate the molar amounts on your reactive...

    fill in reaction table below. Make sure you correctly calculate the molar amounts on your reactive materials. Just need Q2-4 answered please CH3 catalytic HO OH + 2x CH3OH HO3S Figure 1. Reaction Scheme Prelab Questions 1) The Material Safety Data Sheets (MSDS) for all the chemicals involved in this lab are on iLearn. Read these and answer the following questions a) Which chemical is the most dangerous in this lab? b) Explain why you chose your answer for part...

  • These problems relate back to the first step mechanism showed. It is a multi step question so you...

    These problems relate back to the first step mechanism showed. It is a multi step question so your answer will be appreciated ssignment-2 for Chem C342 (Hon) Total points: 50 points Assignment due: Monday, April 19, 2019 (No Excuse 1. Meclizine is an antiemetic. It he Ips p revent or at least lessen the vomiting associated with Meclizine can be synthesized by the following motion sickness, including seasickness. series of reactions: 20 pts Cl он CI CI Cl CH3 Meclizine...

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