(a)
Interpretation: The name of the following structure should be determined.
Concept Introduction: While naming hydrocarbons, we use several prefixes in order to state the total number of carbons present. For example: In propane, butane, pentane, the suffix -ane represents hydrocarbon chain and prefixes, -prop, -but and -pent represents three, four and five carbons in the hydrocarbon chain. Also, if there is any substituent or group present at any position then the naming of hydrocarbon is done in such a way that it represents the position of that substituent. Also, alcohols are common organic groups which contain the hydroxyl group, or OH-.
(b)
Interpretation: The name of the following structure should be determined.
Concept Introduction: While naming hydrocarbons, we use several prefixes in order to state the total number of carbons present. For example: In propane, butane, pentane, the suffix -ane represents hydrocarbon chain and prefixes, -prop, -but and -pent represents three, four and five carbons in the hydrocarbon chain. Also, if there is any substituent or group present at any position then the naming of hydrocarbon is done in such a way that it represents the position of that substituent. Also, alcohols are common organic groups which contain the hydroxyl group, or OH-.
(c)
Interpretation: The structure of methanol should be determined.
Concept Introduction: While naming hydrocarbons, we use several prefixes in order to state the total number of carbons present. For example: In propane, butane, pentane, the suffix -ane represents hydrocarbon chain and prefixes, -prop, -but and -pent represents three, four and five carbons in the hydrocarbon chain. Also, if there is any substituent or group present at any position then the naming of hydrocarbon is done in such a way that it represents the position of that substituent. Also, alcohols are common organic groups which contain the hydroxyl group, or OH-.
(d)
Interpretation: The structure of 2-heptanol should be determined.
Concept Introduction: While naming hydrocarbons, we use several prefixes in order to state the total number of carbons present. For example: In propane, butane, pentane, the suffix -ane represents hydrocarbon chain and prefixes, -prop, -but and -pent represents three, four and five carbons in the hydrocarbon chain. Also, if there is any substituent or group present at any position then the naming of hydrocarbon is done in such a way that it represents the position of that substituent. Also, alcohols are common organic groups which contain the hydroxyl group, or OH-.
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Chapter 9 Solutions
Chemistry For Changing Times (14th Edition)
- Explain why this data led Rayleigh to look for and to discover Ar.arrow_forward5) Confidence interval. Berglund and Wichardt investigated the quantitative determination of Cr in high-alloy steels using a potentiometric titration of Cr(VI). Before the titration, samples of the steel were dissolved in acid and the chromium oxidized to Cr(VI) using peroxydisulfate. Shown here are the results (as %w/w Cr) for the analysis of a reference steel. 16.968, 16.922, 16.840, 16.883, 16.887, 16.977, 16.857, 16.728 Calculate the mean, the standard deviation, and the 95% confidence interval about the mean. What does this confidence interval mean?arrow_forwardIn the Nitrous Acid Test for Amines, what is the observable result for primary amines? Group of answer choices nitrogen gas bubbles form a soluble nitrite salt yellow oily layer of nitrosoaminearrow_forward
- 3. a. Use the MS to propose at least two possible molecular formulas. For an unknown compound: 101. 27.0 29.0 41.0 50.0 52.0 55.0 57.0 100 57.5 58.0 58.5 62.0 63.0 64.0 65.0 74.0 40 75.0 76.0 20 20 40 60 80 100 120 140 160 180 200 220 m/z 99.5 68564810898409581251883040 115.0 116.0 77404799 17417M 117.0 12.9 118.0 33.5 119.0 36 133 0 1.2 157.0 2.1 159.0 16 169.0 219 170.0 17 171.0 21.6 172.0 17 181.0 1.3 183.0 197.0 100.0 198.0 200. 784 Relative Intensity 2 2 8 ō (ppm) 6 2arrow_forwardSolve the structure and assign each of the following spectra (IR and C-NMR)arrow_forward1. For an unknown compound with a molecular formula of C8H100: a. What is the DU? (show your work) b. Solve the structure and assign each of the following spectra. 8 6 2 ō (ppm) 4 2 0 200 150 100 50 ō (ppm) LOD D 4000 3000 2000 1500 1000 500 HAVENUMBERI -11arrow_forward
- 16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してしarrow_forward3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CNarrow_forwardShow work..don't give Ai generated solution...arrow_forward
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