Question

8. Describe the best method for each of the following laboratory syntheses, given a single reactant. Include why you chose th
0 0
Add a comment Improve this question Transcribed image text
Answer #1

The best methods are those which are easy to detect, green and are not sensitive to other functional groups.

Ano Page : Date -REACTION (@існун, ң,-Он _REAGANT PCC CH₂ CH CH CHO ADVANTAGE Pee offers advantage of selective oxidation of

Add a comment
Know the answer?
Add Answer to:
8. Describe the best method for each of the following laboratory syntheses, given a single reactant....
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
  • LABORATORY 8 Post-Lab 1. Explain how each of the following errors would have altered your results....

    LABORATORY 8 Post-Lab 1. Explain how each of the following errors would have altered your results. Clearly explain why your calculated answer would be high, low, or unchanged. (A single word answer is not acceptable.) a. You decided to take the pH after each addition of 5.0 mL of NaOH rather than after every 0.5 mL during the neutralization of your acid sample. b. While using the Half Volume method, your solution was dark pink (you overshot the endpoint) and...

  • Pre-Laboratory Assignment 1. Briefly describe the hazards associated with us ing the following (1) concentrated NH,...

    Pre-Laboratory Assignment 1. Briefly describe the hazards associated with us ing the following (1) concentrated NH, solution 3. We can prepare the yellow coordination compound potassium tris(oxalato rhodate(lll), KIRh(,0)), by reacting potassiumn hexachlororhodatelli), KIRCI. and potassium oxalate, K 0,04 (1) Balance the chemical equation for this reac- tion, shown below. K(RhCi (aq) + K C20 (aq) → K[Rh(C2O4)3 (s. yellow) + KCl(aq) (2) If we combine 1 mol of KIRhClel with 1 mol of K C204, which compound is the...

  • Answer the questions based on following information. 7.     Describe the data collection method(s)'...

    Answer the questions based on following information. 7.     Describe the data collection method(s)' a.     Who collected the data? b.     What tools were used? c.     What were the ethical considerations addressed and discuss gaps you identified. d.     You will need to summarize and analyze the information from the article in your own words Method a quantitative, cross-sectional, descriptive design was chosen for this study. The instrument that was used to collect the data was a self-report questionnaire. a questionnaire previously used...

  • CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectivene...

    please answer all these questions, thank you. CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...

  • Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could...

    Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...

  • need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...

    need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...

  • SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question....

    SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question. 00 OA Figure 2.1 Using Figure 2.1, match the following: 1) Tertiary (protein) structure, 2) Monosaccharide 3) Nucleotide 4) Lipid 5) Functional protein 6) Polymer 7) Polysaccharide TRUE FALSE. Write T if the statement is true and F if the statement is false, 8) Final preparation for cell division is made during the cell life cycle subphase called G2. SHORT ANSWER. Write the word...

  • help with identifiying each unknown in extraction and washing experiment. the ir spectra are given below,...

    help with identifiying each unknown in extraction and washing experiment. the ir spectra are given below, along with data, and the lab sheet is attached. Neutral Solid Primary amine (Aniline) 3403cm - NE presence Transmittance 60 3258cm 1 streren NOUD Streich 50 Ctretcher strator NH2 aromatto 11 NO2 aring 2-nitroaniline K LILI 3600 3200 2800 2400 2000 1800 1600 Wavenumber cm-1 1400 1200 1000 800 600 Basic Solid primary amine Transmittance I NH2 Stretch p-acetvianiline 70 60 CS HG NO...

  • The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There...

    The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are pictures attached of the lab manual. 2) Is this method a good route for the preparation of p-sec-butyltoulene? Give reasons for your answer. 3) Why do you use a large excess of toulene. What are its functions? 4) What is the purpose for adding the hydrochloric acid to the water in the separatory funnel in step 5? Hint: If no acid is added,...

  • Create graphs for Figures 1-4 (circled on pages 111 & 114) based on the data given in Tables ...

    Create graphs for Figures 1-4 (circled on pages 111 & 114) based on the data given in Tables 2 & 4. Lab # 8 Cellular Respiration and Fermentation I. Goals and Objectives At the completion of this laboratory exercise, students will be able to: A Differentiate between the intermediates and products of fermentation versus acrobic cellular respiration in yeast. Relate rates of fermentation with sugar availability in yeast. Utilize a reduction-oxidation dye to determine the effect of varying yeast concentration...

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