18. Indicate which products would be obtained from the chlorination of 1,5-hexadiene at high temperature (500°c), using a 1:1 mole ratio of the reactants. CICH2CHCH2CH2CH=CH2 CICH2CH=CHCH=CHCH2CI CI I CICH2CH=CHCH2CH=CH2 III CH2=CHCH2CHCH=CH2 a) I and II b) II and III c) III and IV d) IV and V e) V and I II CICH2CHCH2CH2CHCH2CI CI CI CI IV V

18. Indicate which products would be obtained from the chlorination of 1,5-hexadiene at high temperature (500°c), using a 1:1 mole ratio of the reactants. CICH2CHCH2CH2CH=CH2 CICH2CH=CHCH=CHCH2CI CI I CICH2CH=CHCH2CH=CH2 III CH2=CHCH2CHCH=CH2 a) I and II b) II and III c) III and IV d) IV and V e) V and I II CICH2CHCH2CH2CHCH2CI CI CI CI IV V

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

10) Synthesis: Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. Br CH3 Br CH3
Draw the line-angle formula of the enol formed in the following alkyne hydration reaction and then draw the structural formula of the carbonyl compound with which this enol is in equilibrium. -C=CH 1. (sia)2BH 2. NaOH/H₂O₂ an enol carbonyl compound • You do not have to consider stereochemistry. • Draw both the enol and the carbonyl forms. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures using the sign from the drop-down menu. ChemDoodleⓇ <
Provide the principle organic product(s) for the following reactions. If more than one product is expected, indicate the major one. Include stereochemistry as appropriate.
X Upon ozonolysis, Compound X produces two compounds: Compound Y and Compound Z. Compound Y can also be prepared from the following synthetic route: PCC 1. R₂BH, THF 1. Mg. Et₂O PCC Compound Y 2. CH₂Cl₂ 2. NaOH, HO CH₂Cl₂ 3. H₂O* From this information, draw the structures of Compounds X, Y, and Z. For Compounds X and Z, different substituents are possible. For grading purposes, just use hydrogens as the substituents. Br مرد →] ►
Draw the products of the three step reaction sequence shown below. Ignore inorganic byproducts. If the reaction results in a mixture of ortho and para isomers, draw only the para-product.
Describe how 1-ethylcyclohexanol can be prepared from cyclohexane. You can use any inorganic reagents, any solvents, and any organic reagents as long as they contain no more than two carbons.
Show how to convert ethylene to 2-Chloroethanol compound.
Write the structure of the major products in the following reactions and name them.
NAME and DRAW the STRUCTURE of ALL the alkenes which could undergo catalytic hydrogenation at 900°C to form methylcyclopentane. Circle the alkene with the HIGHEST stability and X the alkene with the HIGHEST heat of hydrogenation. Give reasons for your choice.
Two substitution products result from the reaction between 3-chloro-3-methyl-1- butene with sodium acetate (CH3COO – Na +) in acetic acid under SN1. Identify the products.
What is the major organic product obtained from the following reaction? H₂Cr₂O7 H₂SO4, H₂O OH A) 1-butene, CH3CH2CH-CH₂ B) butanal, CH3CH₂CH₂CHO C) butanone, CH3CH₂COCH3 D) butanoic acid, CH3CH2₂CH₂COOH
0 CH₂ → ?? If the above compound is subjected to combustion, what are the products? ethanoic acid +2-phenyl-ethene-1-ol 15CO₂ (g) + 5H₂0 (g) O 2-phenyl-ethyl-ethanoate + H₂O 20CO₂ (g) + 10H₂O(g) →?? CH, if the above compound was treated with H and H₂O what product will form?