### Gas Chromatography Analysis of Isomeric Butenes**Question**What is the relative percent yield of the major product of the three isomeric butenes analyzed via the GC analysis from Units 9 and 10? [Enter a value with 3 significant figures and without the % sign]**Chromatogram Analysis**A chromatogram is provided with an intensity (y-axis) versus retention time (x-axis) graph. The data file path is: ```C:\GCsolution\Data\CH337 units 9, 10\Spring2016\TueLab_12_XXXXX.g```The peaks observed on the chromatogram correspond to different isomeric butenes. The retention times and the intensity give an indication of the presence and quantity of each compound.**Peak Table - Channel 1 Details**Below the chromatogram, there is a peak table:| Peak# | Ret. Time | Area | Height | Name ||-------|-----------|------|--------|------|| 1 | 2.353 | 4524 | 2730 | || 2 | 2.421 | 17950| 10853 | || 3 | 2.479 | 5569 | 3276 | || **Total** | | **28043** | **16859** | |### Calculation of Relative Percent YieldTo find the major product’s relative percent yield, you need to compare the area under the major peak (Peak 2) to the total area of all peaks.- **Area of Major Peak (Peak 2)**: 17950- **Total Area**: 28043**Relative Percent Yield of Major Product**:\[\frac{17950}{28043} \times 100 = 63.98\%\]Therefore, the relative percent yield of the major product is **63.98** (to three significant figures: **64.0**).### Interpretation- **Retention Times**: Indicate the time taken for each compound to pass through the chromatographic column.- **Areas under Peaks**: Proportional to the amount of each compound present in the sample.Understanding the retention times and peak areas can help identify the compounds and their relative concentrations in the mixture.For more details on interpreting GC data, please refer to the relevant sections of Units

Percentage yield of any species A in GC chromatogram is = ( peak area of A/total area)*100…

Answered: What is the relative percent yield of…

What is the relative percent yield of the major product of the three isomeric butenes analyzed via the GC analysis from Units 9 and 10? [

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

Liquid hexane (CH;(CH,) CH;) will react with gaseous oxygen (O2) to produce gaseous carbon dioxide (CO,) and gaseous water (H,0). Suppose 5.2 g of hexane is mixed with 10.6 g of oxygen. Calculate the maximum mass of water that could be produced by the chemical reaction. Round your answer to 3 significant digits. do
Draw the structure of the organic product of the reaction between cyclohexene and H₂, Pd/C. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Separate multiple products using the + sign from the drop-down menu. . In cases where there is more than one answer, just draw one.
2. Between the chlorination and bromination (with light) of 2-methylpropane (HC(CH3)3), explain which reaction will have greater selectivity. Assume the hydrogen abstraction in chlorination is exothermic whereas for bromination is endothermic. You may use diagrams to help with your explanation.
QUESTION 17 Ignoring isotope effects, after one E2 elimination with ethoxide, which bromine will predominate in the cyclohexene product? Explain your choice in 50 words or less. CH3 81B. H3C - 79B. H- t-Bu- H. For the toolbar, press ALT+F10 (PC) or ALT+FN+F10 (Mac). ABC 3(12nt) !! TTT Arial Save All Answers Click Save and Submit to save and submit. Click Save All Answers to save all answers. scroll to see more
Please don't provide handwritten solution .....
3. If both water and your alkene products distill into your collection flask, why might you get two layers? because there is a temperature gradient in the graduated cyclinder because methylcyclohexenes and water are immiscible because methylcyclohexenes and water are miscible
WHich statement is true? Statement 1: When Sodium Detection for Active Hydrogen test was conducted with 2-butyne, hydrogen gas will be produced. Statement 2: When alkene is subjected to Baeyer's Test for Unsaturation, the formation of a brown suspension will be observed. This is due to the presence of MnO2 which is the reduction product of the confirmatory reagent KMnO4.
Identify the best conditions to dihydroxylate an alkene to the trans-diol. A) KMnO, NaOH (pH >8), cold B) KMnO, NaOH (pH >8), warm C) mCPBA followed by acidic aqueous workup D) OSO (catalytic), NMO E) 1.OsO, 2. Nalo, 3. Na₂S₂O,, H₂O 4
Discuss the structure of ethyl chloride, its nomenclature (systematic and common), it's physical properties, method/s of preparation, and applications .
5. Write stepwise equations (balanced where possible) for the syntheses of the following compounds. As there is more than one "right" answer, be sure to include special requirements and conditions where appropriate. Please keep the use of BF&I to a minimum. a. NaBH, from B(OME), 1- b. B.Hg from diborane(6) c. SiCl4 from SiO₂ d. Ca(CH3)2
Please can you help me with this question.
Question 4 For the indicated reaction, determined which compounds listed would be the most reactive. Reactivity towards 15% Nal/Acetone solution: Can not use subscripts in the answers so C,H5CH3 = C2H6CH3. %3D O ArCI O (Ar)2CHCI ARCH2CI (Ar)3CCI Question 5