**Educational Text and Explanation:****CHM 2070 Lab - Fall 2020****Compound Analysis and Chromatography****d.** You are given a mixture of three compounds (A, B, C, as shown below):- Compound A: Naphthalene derivative with a methyl group (CH₃)- Compound B: Naphthalene derivative with a hydroxyl group (OH)- Compound C: Naphthalene derivative with a methoxy group (OCH₃)**a.** **Rank the three compounds from least to most polar:**- A (least polar) → C → B (most polar)---**b.** You conduct a Thin Layer Chromatography (TLC) experiment on this mixture and obtain the TLC plate shown on the left. Identify all three compounds on the TLC plate:- The TLC plate is divided into three columns representing different solvent polarities.- The left column is with the original solvent showing three distinct spots at varying heights.**c.** **What would the TLC plate look like if you used a less polar solvent?**- In the middle column ("less polar solvent"), the spots would be lower on the plate compared to the original as the compounds do not move as much.**d.** **What would the TLC plate look like if you used a more polar solvent?**- In the right column ("more polar solvent"), the spots would be higher on the plate as the compounds travel further with a more polar solvent.**e.** **Calculate the Rf value of the middle spot of the first plate.**- Use a ruler to measure the distance traveled by the middle spot and divide it by the total distance traveled by the solvent front to calculate the Rf value. (Rf = distance traveled by compound / distance traveled by solvent front)**f.** **In what order would the three compounds elute in column chromatography?**- **Order to elute:** - First to elute: A - Middle: C - Last to elute: BThis activity demonstrates the use of TLC to determine the polarity of compounds and the effect of solvent polarity on the separation process. Understanding the order of elution is crucial for effective separation and purification in column chromatography.

a)polarity in increasing order A. C. B. b)top one spot is for A middle spot is for C and…

d. You are given a mixture of three compounds (A, B, C, below). он CH, осн, в A a. Rank the three compounds from least to most polar. A в least polar most polar CHM 2070 Lab Fall 2020 b. You conduct a TLC experiment on this mixture and obtain the TLC plate shown below on the left. Identify all three compounds on the TLC plate

d. You are given a mixture of three compounds (A, B, C, below). он CH, осн, в A a. Rank the three compounds from least to most polar. A в least polar most polar CHM 2070 Lab Fall 2020 b. You conduct a TLC experiment on this mixture and obtain the TLC plate shown below on the left. Identify all three compounds on the TLC plate

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Hello, can you help me with this question? Please make sure your answer is not wrong. Thank you.
Help pls
Highlight in red the 2° carbons in this molecule. Highlight the 3° carbons in blue. OH CI X G A
From the image of the pigments above, which is more polar? Why?
all parts of the same question
CI H FC H The compound shown above has the molecular formula C2H5CI. Identify any structure(s) below that represent(s) another representation of the compound shown above. Do NOT select any constitutional isome of the compound above. Select all answers that apply. А. H С. CI H FC C CI H- C С —Н H H H CI H H- H -C H- H CI А. C. D. none of the above D. B. B.
ge 2: e 3: 4: Listen Record your answers on a separate piece of paper. Be sure to draw the structure next to your answers and point to the carbon you're assigning designation to. Immediately following the test upload your answers. DO NOT skip forward, you will not be able to come back to this question. Label EACH asymmetric carbon (stereogenic carbon) in the molecules below as having R or S configurations. CI = Br Br ле COOH H Br OH Br- H H "NH2 CHO
For the substituted cyclohexane compound given below, highlight the groups – by clicking on atoms – that are cis to the hydroxyl (OH) substituent. CH3 Br F. но
Draw A to G structure.
Identify the following compounds if they are alkane, alkyne, alcohol or ether. Note: need answers immediately. Will send a good rate right away as well.
Make the following changes on the molecule in the drawing area below: 1. First, make sure this is the B anomer. Edit the molecule if necessary. 2. Then replace the hydroxyl group on carbon #4 with a chlorine atom. H K ОН CH,ОН H ОН H H ОН ОН Н
C31 H5y 2. Compound X, reacts with excess H/Pd to give C31 Hoo How many double bonds and how many rings are in X? Show your work. 150 3 APR étv 1 MacBook >> D00 000 20 F8 F9 F7 F6 F5 F3 F4