10- For the following scheme, if the center compound alkene as shown, Give one actual example for the conversion of this alkene to these shown compounds: Alcohol, alkane, diol, dihalides, etc. Show the condition, of temperature, pressure, and the catalysts needed (if any) for each reaction. OH Halohydrin ** 1,2-Dihalide Halide H OH Alcohol Alkene Alkane Epoxide HO он 1,2-Diol C=O Carbonyl compound Cyclopropane

10- For the following scheme, if the center compound alkene as shown, Give one actual example for the conversion of this alkene to these shown compounds: Alcohol, alkane, diol, dihalides, etc. Show the condition, of temperature, pressure, and the catalysts needed (if any) for each reaction. OH Halohydrin ** 1,2-Dihalide Halide H OH Alcohol Alkene Alkane Epoxide HO он 1,2-Diol C=O Carbonyl compound Cyclopropane

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...

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4. A hydrocarbon of unknown structure (ooh, you're gonna LOVE OCII!!!) has the molecular formula C3H10. When treated with rhodium during catalytic hydrogenation, three molar equivalents of hydrogen are absorbed. When this unknown hydrocarbon is treated with CACO3 and H2/Rh, only ONE molar equivalent of hydrogen is absorbed. a. Draw two structures for this unknown that fits the data given. b. Are there rings present? c. Any double/triple bonds? d. How many degrees of unsaturation does this unknown have? e. Could it possess a BENZENE ring, which IS unsaturated AND has a RING...
a-pinene When a-pinene reacts with 1. BH3; 2. H₂O2, NaOH, H₂O 4 possible cis,trans isomers can be formed, but one of these is formed more readily than the others. Draw the structure of this preferred isomer. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • To aid you in your drawing, the structure of a-pinene is provided for you in the drawing palette.
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LS THE LOTIOmpus and us Mos e sono cobonug DISM (AOL BLGISLLEQ (ABS): ONIS I CHWJ3J a. T-120biobA1-5-logoccioburgue *CH-CH³ 5. First indicate the classification of alcohol (primary, secondary or tertiary), then using the classification, draw the aldehyde, ketone, carboxylic acid or no product formed when most oxidation reactions the following alcohols are mildly oxidized. *keep in mind there is a byproduct of water in b. V H H OH H-C-CC-H H H H Classify the alcohol: 1°, 2° or 3⁰ ОН Classify the alcohol: 1°, 2° or 3⁰ 1. [0] [0] DAHOAM CPSLER 8 10se
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please help with the following OChem question 1. Provide the bond line structures and the IUPAC names for the major organic products formed in each step of the following reaction scheme (see attached image)
Organic chemistry student Karen is tasked with synthesizing (S)-3-methylbutan-2-ol. Using her knowledge of alkene reactions, she runs a hydroboration/oxidation reaction on 2-methylbut-2-ene. Upon isolation, Karen runs an optical rotation experiment to determine the enantiopurity of her alcohol. Which of the following statements would be MOST correct regarding the optical rotation of her synthetic sample (Note: the specific rotation of (R)-3-methylbutan-2-ol is -40.4°). O [x] of the sample will be 0° O [x] of the sample will be -40.4° O [x] of the sample will be between 0° and -40.4° O [x] of the sample will be between 0° and +40.4° [x] of the sample will be +40.4°
9. Read very carefully: Alkenes can be OXIDIZED to form carbonyl compounds (- C=0) (see example below). KNOWING this, how would you distinguish the following two alkenes by using this OXIDATIVE reaction? R-CH=CHCH3 à (oxidation) R -CO,H + CH;CO,H BOTH undergo OXIDATION
Answer both questions below: Give the systematic names of the isomers A, B, C, & D and arrange the compounds A, B, C & D in order of increasing boiling point, commencing with the one having the lowest boiling point. Hence explain the physical basis of the order you gave. Draw a labelled energy profile for the hydrolysis of compound A
Organic chemistry student Peter is tasked with synthesizing (R)-3-ethylpentan-2-ol. Using his knowledge of alkene reactions, he runs a hydroboration/oxidation reaction on 3-ethylpent-2-ene. Upon isolation, Peter runs an optical rotation experiment to determine the enantiopurity of his alcohol. Which of the following statements would be MOST correct regarding the optical rotation of his synthetic sample (Note: the specific rotation of (S)-3-ethylpentan-2-ol is +28.2°). O [x] of the sample will be +28.2° O [x] of the sample will be 0° O [x] of the sample will be between 0° and -28.2° O [a] of the sample will be -28.2° O [x] of the sample will be between 0° and +28.2°