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...

See similar textbooks

Similar questions

Draw a structural formula for butanoic acid. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. ● 0-0 Ste 9-85 // CH4 to access importan [ ] کر ? ChemDoodleⓇ
Ethanol, isopropyl alcohol, and n-propyl alcohol may all be used as ingredients in hand sanitizer. Which of those three could be made most easily by reduction of acetone (CHCOCH3) with a hydride reagent?
Chemistry the question numbers are in the top left corner of each picture. some questions have more than one picture. thanks!!!
12. Which of the following carbocations is the least stable one? 13. The heats of complete hydrogenation of the following three hydrocarbons are 105, 116, 275 and 292 (in kJ/mol). Which hydrocarbon does feature the heat of hydrogenation of 292 kJ/mol?
Please answer all questions. This is all the information
Give the organic product: DỊCH I Bry Febr *HO-O: O-CHa " AKCI remove any ortho product that forms at this point. II Zn(Hg) HEAT гноо: Br :ö CH: OH 13
Organic Chemistry (major/minor products + type of reaction)
(a) • Consider E/Z stereochemistry of alkenes. • Do not show stereochemistry in other cases. • You do not have to explicitly draw H atoms. Draw a structural formula for the alkene: 2-methyl-2-heptene. MUIL Templates Sn [F ? Ⓡ ChemDoodle (b) Draw a structural formula for the alkene: (E)-1-chloropropene.
NS Predicting the reactants or products of alkene hydration Give one possibility for the mystery reactant R in this organic reaction: OH H+ R+H20 Specifically, in the drawing area below draw the skeletal structure of what R might be. There may be more than one reasonable answer. c+ II
Write the structure(s) for the organic product(s) of the carbohydrate reaction below. ball & stick v|- + labels HOCH2 CH3 0-Ć-CN dilute aq. HCI HO. ČH3 OH Linamarin • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If two diastereomers are formed, draw both. • If no reaction occurs, draw the organic starting material. • Draw carboxylic acids in neutral (unionized) form. • Use “flat" representations of rings, not chairs, in your drawing. Do not draw your answer as a Haworth projection.
Give the systematic (IUPAC) name for the following compounds. Include stereochemistry in the name ONLY FOR THOSE STRUCTURES THAT ALLOW YOU TO DETERMINE STEREOCHEMISTRY. In other words, describe the stereochemistry if the molecule is shown as a Fisher projection, or as a perspective formula, or if an alkene is drawn with the correct stereochemistry representation