Compound X is developed on a TLC plate using a 3:1 heptane:acetone eluent mixture. The same compound is then developed on a fresh TLC plate using a mixture of 1:3 heptane:acetone eluent mixture. Select all the correct answers. A. Compound X will have a larger Re value in the 1:3 heptane:acetone eluent mixture. B. Compound X will travel closer to the solvent front in the 1:3 heptane:acetone eluent mixture. OC. Compound X will have the same Ry value in both eluent mixtures. D. Compound X will have a larger R, value in the 3:1 heptane:acetone eluent mixture.
Compound X is developed on a TLC plate using a 3:1 heptane:acetone eluent mixture. The same compound is then developed on a fresh TLC plate using a mixture of 1:3 heptane:acetone eluent mixture. Select all the correct answers. A. Compound X will have a larger Re value in the 1:3 heptane:acetone eluent mixture. B. Compound X will travel closer to the solvent front in the 1:3 heptane:acetone eluent mixture. OC. Compound X will have the same Ry value in both eluent mixtures. D. Compound X will have a larger R, value in the 3:1 heptane:acetone eluent mixture.
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question is about a TLC analysis of spinach pigments
![Compound X is developed on a TLC plate using a 3:1 heptane:acetone eluent mixture. The same compound is then developed on a fresh TLC plate using a mixture of 1:3
heptane:acetone eluent mixture. Select all the correct answers.
A. Compound X will have a larger Rf value in the 1:3 heptane:acetone eluent mixture.
B. Compound X will travel closer to the solvent front in the 1:3 heptane:acetone eluent mixture.
C. Compound X will have the same Rf value in both eluent mixtures.
D. Compound X will have a larger Rf value in the 3:1 heptane:acetone eluent mixture.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F297f3ac9-0b45-4f0e-a4c7-c62f78084607%2F4c3d63a4-ad4d-493f-abb2-897cbeeff4a9%2Fz7u2jfn_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Compound X is developed on a TLC plate using a 3:1 heptane:acetone eluent mixture. The same compound is then developed on a fresh TLC plate using a mixture of 1:3
heptane:acetone eluent mixture. Select all the correct answers.
A. Compound X will have a larger Rf value in the 1:3 heptane:acetone eluent mixture.
B. Compound X will travel closer to the solvent front in the 1:3 heptane:acetone eluent mixture.
C. Compound X will have the same Rf value in both eluent mixtures.
D. Compound X will have a larger Rf value in the 3:1 heptane:acetone eluent mixture.
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