**Question 25:** What is the formula of the main product formed when an addition reaction takes place between cyclohexene (C₆H₁₀) and water, catalyzed by H₂SO₄?**Options:**a. Cyclohexanol- ![O]( image of a cyclohexane ring with an -OH and -CH₃ group attached)b. 1-Methylcyclohexanol- ![O](image of a cyclohexane ring with an -OH group attached)c. 2-Methylcyclohexanol- ![O](image of a cyclohexane ring with two -OH groups attached)d. Cyclohexanone- ![O](image of a cyclohexane ring with a -C=O group attached)e. No correct response**Answer Explanation:**In an addition reaction of water to an alkene like cyclohexene, in the presence of an acid catalyst such as sulfuric acid (H₂SO₄), an alcohol is typically formed. The most likely product is 1-methylcyclohexanol, where the double bond in cyclohexene is broken and an -OH group is added, usually following Markovnikov’s rule.

Answered: Image /qna-images/answer/4899a693-d28d-4aba-80a8-0f12d5742e6d.jpg

Answered: 25. What is the formula of the main…

25. What is the formula of the main product formed when an addition reaction takes place between CH and water, catalyzed by H,SO? CH Oa. CH Ob. OH CH OH Oc. Od. C-OH O e. no correct response

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

Exercise: Ketone A can be converted to alkene B in a one-step reaction via route I. It can also be converted to alkenes B and C via nucleophilic addition with a Grignard reagent followed by dehydration reaction with sulfuric acid in route II. CH2 Route I Ketone, A Alkene, B 1. CH,MgBr, H,O 2 H,SO, heat Route II Alkenes, B and C a) Provide a suitable reagent for the conversion of ketone A to alkene B in route I above. b) Suggest the structure of the intermediate in route Il and write a mechanism for the reaction of ketone A with the Grignard reaction. c) Draw the structure of alkene C and identify which alkene is the major product in route II. d) If you were assigned to synthesize alkene B from ketone A, which route would you use for the synthesis? Provide reasons for your choice of synthesis.
What is the major 1,4 product for the following reaction? X Selected Answer Answers: H-Bri Br Br- Br Br Br 7
Predicting the reactants or products of esterification hat is the missing reactant in this organic reaction? H R+ OH Ο + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reaso drawing area. Explanation Check Ο O 2 $ % 5 7 8 X
Exercise 6 1. Classify the following carbocations in order of stability, justify: CH3-CH2-CH2 ® ; CH3 ® ; C6H5-CH2 © ; CH3-CH2 ® ; (CH3)3CO ; CH3-CHO-CH3 2. Classify the following carbanions in order of stability, justify: 3. CH3-C(OO)=CH-CH=CH-NO2 ; CCI3 O ; CH2CIO ; CHCI2
tab esc app.aktiv.com ! 1 Draw the two products of the reaction shown below. Assume only 1 equivalent of HI is consumed in this reaction. Ignore any inorganic byproducts. F1 H3C Q Edit Alco Product 2 HI F2 S W #3 80 F3 $ E $ 4 F4 3 S % R 07 2⁰ a 5 F5 Problem 29 of 5 < 6 T FG & Y
EXERCISE Electrophilic Addition: Propene Hydrochlorination Click on a basic (nucleophilic) atom. HH HIC-CIC H Recheck 1st attempt H Submit Answer H :: H-CI: Next (1 of 8) Although this chlorine has lone pairs, like other univalent chlorines, it is a very weak Brønsted base and nucleophile. Try again. Try Another Version cengagenow.com/ilm/global/tech Support.do 3 item attempts remaining Cengage Learning I Cengage Techesion ABU:
Outcome 11 Evaluation: Bridge Assignment #1 Predicting Products of EAS with Directing Groups 1) Just like I did in the video for addition of Bromine to Toluene, draw the intermediate resonance structures and final product for the addition of Chlorine to Phenol at all three possible positions ( m, and p). You are adding chlorine once in each reaction below, just at different spots: a. Addition of Cl ortho to the OH (there will be four intermediate resonance structures): OH он AICI, b. Addition of Cl meta to the OH (there will be three intermediate resonance structures): OH он AICI, с. Addition of Cl para to the OH (there will be four intermediate resonance structures): OH OH AICI,
Exercise 25. Determine the mechanism of nucleophilic substitution of each reaction. Draw the products, including stereochemistry. 1. "OCH3 DMSO Br H. CI CH3CH2OH + 2.
Problem 10-6 Dimethylamine, (CH3)2 NH, has a molecular weight of 45 and a boiling point of 7.4 °C. Trimethylamine, (CH3)3N, has a higher molecular weight (59) but a lower boiling point (3.5 °C). Explain this apparent discrepancy.