QUESTION 8H2SO4,Compound A(Intermediate enol)Compound B(Final product)+ H20HgSO,a) Predict the structural formula for compound A and B.te Nb) Identify the function of concentrated H2S04 and HgSO4.

Answered: Image /qna-images/answer/6651ac5c-a1fe-44fc-8c0e-53b3ff66597f.jpg

QUESTION 8 H2SO4. H9SO4 Compound A (Intermediate enol) Compound B (Final product) + H20 a) Predict the structural formula for compound A and B. b) Identify the function of concentrated H2S04 and HgSO4.

QUESTION 8 H2SO4. H9SO4 Compound A (Intermediate enol) Compound B (Final product) + H20 a) Predict the structural formula for compound A and B. b) Identify the function of concentrated H2S04 and HgSO4.

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

What starting material is needed to form a secondary alcohol using H2/Pt? A. Aldehyde B. Ester C. Amide D. Alkene E. Ketone F. Carboxylic acid 2. Which starting material is/are a needed to form an anode and water using the reagent H+/ heat ( choose all that apply) - carboxylic acid - amine - ketone -aldehyde -carboxylate ion -ammonium ion alcohol
In the following acid - base reactions, a) Draw Lewis structures of the reactants and the products. b) Determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). c) Use the curved - arrow formalism to show the movement of electron pairs in these reactions and the imaginary movement in the resonance hybrids of the products. d) Indicate which reactions are best termed Brønsted-Lowry acid - base reactions i. CH3CHO + HCI-- > CH3CH2O + + Cl- ii. CH3CHO + OH- - - > CH3CO-(OH) H
2. What type of chemical reaction is illustrated by the following reaction? CH3OOCH3 + H2O ⎯→ CH3OOH + CH3OH a. oxidation/reduction b. substitution c. neutralization d. hydrolysis e. dehydration synthesis (condensation)
7 8. 9 10 11 1. 4 28 29 30 31 32 33 34 35 36 37 38 39 23 24 25 26 27 45 46 47 48 49 50 A MoVing to another question Will save this response. Question 11 What is the major organic product obtained from the following reaction? OH OH OH OH 4 O a.1 O b.2 OC. 3 O d.4 A Moving to another question will save this response. P Type here to search 42 Esc F1 F2 F3 F4 F5 F6
20. In the IUPAC name for the following compound, the -Br group is located on carbon number_? CH;CHCH=CH, Br a. 1 b. 2 С. 3 d. 4
Consider propanoic (CH3CH2CH2CO2H) acid and pentanoic (CH3CH2CH2CH2CO2H) acid and the corresponding alcohols with the same number of carbons, propanol (CH3CH2CH2COH) and pentanol (CH3CH2CH2CH2COH). Select the class of compound that is more soluble. {one answer] Select the best explanation for your answer to the previous question. [a second answer] Group of answer choices a. The solubility of alcohols in water decreases with increasing chain length. b. Propanoic acid and pentanoic acid are more soluble in water than the corresponding alcohol. c. Carboxylic acids are generally more soluble in water than alcohols of the same chain length because of increased hydrogen bonding with the -COOH functional group. d. Propanol and pentanol are more soluble in water than the corresponding carboxylic acid e. The solubility of carboxylic acids in water decreases with increasing chain length. f. Alcohols are generally more soluble in water than carboxylic acids of the same…
5. Synthesis of aspirin a. Write the sequence of reactions to produce aspirin using salicylic acid, acetic anhydrous, and phosphoric acid.
11- Choose the correct statement: to Dat (i) (ii) (iii) (iv) A. (iii) and (iv) are chain isomers B. (i) and (iv) are functional isomers C. (ii) and (iv) are chain isomers D. (i) and (ii) are functional isomers 12- Choose the common name for the following molecule: A. 3-Methylbutanone B. 2-Methylbutanone C. Methyl propyl ketone D. Isopropyl methyl ketone 13-(CH3)2CHCHO is the final product resulting from oxidation of X in presence of Y. What are X and Y? A. X: Isobutyl alcohol and Y: CrO3/H2SO4(aq) B. X: sec-Butyl alcohol and Y: PCC/CH₂Cl2 C. X: Isobutyl alcohol and Y: PCC/CH₂Cl2 D. X: sec-Butyl alcohol and Y: CrO3/H2SO4(aq)
A student found an unknown solution which had the distinct odor of an organic compound. In an attempt to identify the functional group, she performed several of the tests used in Experiment # 6. The observations are tabulated below. a. Primary alcohol b. Carboxylic acid c. Tertiary alcohol d. Secondary alcohol e. Aldehyde f. Ketone Reagent Color of control sample Color after the test Potassium dichromate (K2Cr2O7) Orange Green Potassium permanganate KMnO4) Deep Purple Brown precipitate Brady's Reagent (dinitrophenylhydrazine) Red-orange solution Deep red precipitate Legal's reagent (sodium nitropruside) Bright red solution No change observed; no precipitate either
7. H3C-CH The compound above is classified as a(n) alkane d. ketone alkene a. e. b. carboxylic acid c. akdehyde 8. Which of the follow ing is a secondary alcohol? d. CH3OH a. H3C C CH3 CH3 b. H3C0-CH3 e. CH3CH2OH c. OH H3C CH3 H. 9. CH3 OH -CH-CH-CH, H3C What is the correct name for the above compound? a. 2-methyl-3-butanol b. 2-pentanol isobutanol d. 3-methy-2-butanol none of these e. c.
2. Alcohols Write the complete step-by-step mechanism for the reaction of 3-methyl-2-pentanol with sulfuric acid.
1. Draw the chemical structures of both Amiodarone and Levothyroxine. Label all of the organic chemical reactions between them (you can use arrows, etc to do this). Aswell as explain Goitre in your own words, the increased iodine from the Amiodarone and why TSH may increase and T3, T4 remain normal etc. -0-CH2 -CH2-N Amiodarone C;H5 CH2)3 CH3 но NH2 Levothyroxine HO. HO. ÑH2