Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Question
A piece of filter paper is placed in the TLC developing chamber to:
Choose one:
provide a lining for the TLC plate to rest on.
help the chamber saturate with the developing solvent's vapor.
make it easier to visualize the solvent front level.
protect the TLC plate.
Expert Solution
arrow_forward
Step 1
The correct option is (c)
It is because filter paper in used in developing chamber as it absorbs the liquid in the solvent and provides more and more surface area of evaporation. So, it help the chamber saturate with the developing solvent's vapour.
Step by stepSolved in 2 steps
Knowledge Booster
Similar questions
- A sample is run on a TLC plate and gives a single spot as shown below on the left. However, the solvent was not allowed to run up the plate very far, and so the experiment was repeated with a much larger solvent distance as shown on the right below. What would be the approximate Rf value of the spot for the repeat experiment on the right? solvent line solvent line start line start line 01.0 0.9 © 0.5 0.1arrow_forwardcomplete the table Procedure Preheat the hotplate stirrer with an aluminum block to 45–50 °C (do not exceed 55 °C). To a clean 5-mL conical vial equipped with a Teflon-coated magnetic stir vane, add 4- bromo-nitrobenzene (152 mg, 0.750 mmol, 1 equiv) and THF (150 μL). Cap the vial and stir the mixture at 45–50 °C for about 30 s to partially dissolve the substrate; don’t stir too fast to avoid splashing the contents on the walls of the vial. Add ammonium chloride (120 mg, 2.2 mmol, 3 equiv), carbonyl iron powder (CIP; 210 mg, 3.80 mmol, 5 equiv), the solution of TPGS-750-M (2% in water, 1.5 mL), and 1 drop of concentrated HCl. Cap the vial and place it on the hot plate stirrer, stirring at 45–50 °C. While the reaction mixture is stirring, prepare an approximate 2% solution of the reactant in DCM (1 sample per 3–4 students) by dissolving 10–15 mg of 4-bromo-nitrobenzene in 0.5 mL of methylene chloride. Prepare the solvent mixture for the mobile phase (25% ethyl…arrow_forwardAs solvent polarity increases, the Retention Factor (Rf) of compounds on the TLC plate increases. Group of answer choices True Falsearrow_forward
- (Solution BII) Prepare 25.00 mL of ~4.000x10-4 M KMnO4 solution via dilution of Solution BI (~0.00100 M KMnO4). Using the appropriately sized volumetric pipet, transfer the required amount of your solution from (BI) into a 25.00 mL volumetric flask. Fill it to the mark with distilled water, stopper it and invert several times to mix. Measure the absorbance of this solution at wavelength of 530 nm, the wavelength where this compound absorbs light most strongly. (e = 2.098 x 103 dm3/mol cm) Calculate the molarity of solution BII Volume of stock BI added via pipettearrow_forwardSuppose you are going to perform a TLC experiment, which materials will you use to prepare the TLC development chamber? Select one or more: Stir bar Funnel Filter paper Beaker Watch glass Erlenmeyer flaskarrow_forwardThe TLC plates below show authentic samples of salicylic acid in the left lane and student product in the right lane. The plate on the left was run in 50:50 hexane:ethyl acetate, and the plate on the right was run in 50:50 hexane:ethyl acetate plus a single drop of acetic acid in the solvent. Calculate the Rf of salicylic acid on the LEFT-HAND PLATE ONLY. Report your answer to two significant figures. 6mm 50:50 41 mah 6mm (45 mm 11:1 11.5mm 50:50 Idrop glacial a.a.arrow_forward
- How can you remove insoluble impurities during a recrystallization? options: 1-Hot gravity filtration. 2- Vacuum filtration 3- It is not possible.You should choose another separation method. 4- Pick out the impurities with tweezers.arrow_forward4. In which step does the liquid in the system become a low-pressure gas? a. Step 1: Compressor b. Step 2: Condenser Coil C. Step 3: Expansion Valve Step 4: Evaporator Coil d.arrow_forwardIn normal phase TLC, the mobile phase is + polar than the stationary phase. Consider the TLC plate below, which was developed using a 25% ethyl acetate:hexane solution. If this same mixture of compounds was developed on a TLC using a 50% ethyl acetate:hexane solution, the orange spot would A mixture of two compounds was developed on a TLC plate. The result is shown below. What is one thing the chemist can do to get better results? In normal phase TLC, the mobile phase is : polar than the stationary phase. Consider the TLC plate below, which was c exane solution. If this same mixture of compounds was developed on a TLC using a 50% ethyl acetate:hexane solution, the orange spot would less sometimes more, sometimes less more A mixture of two compounds was developed on a TLC plate. The result is shown below. What is one thing the chemist can do to get better results?arrow_forward
- Which is more accurate, a transfer pipet or a measuring pipet? What is theuncertainty in microliters when you deliver either 10 mL or 100 mL from a 100-mL adjustable micropipet?arrow_forwardA TLC plate showed two spots A and B with Rf 0.20 and 0.30, respectively. Sketch a TLC chromatogram with the above Rf values. (Hint: Start with a 10-cm TLC plate and allow 1 cm each for the start and end solvent fronts.) Determine the distances travelled from the start of the solvent front. ___?____ A ____?___ B Determine the distances left to the end of the solvent front. ___?____ A ____?___ Barrow_forwardA lower and/or broader melting point range for a compound after recrystallization most likely results from ________. insoluble impurities such as dust or lint the material still being wet with the recrystallization solvent the compound decomposing in the heated solvent the compound undergoing a chemical reaction with the solventarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY