An unknown organic compound is tested with bromine solution. The red color of bromine disappears. Select the possibilities that may be present. Note: You may have to select more than one option. Select 3 correct answer(s) | Water insoluble phenol A phenol in which there are substituents on ortho and para positions Unsaturated hydrocarbon (Alkene or alkyne) Aromatic amine Simple water soluble phenol

An unknown organic compound is tested with bromine solution. The red color of bromine disappears. Select the possibilities that may be present. Note: You may have to select more than one option. Select 3 correct answer(s) | Water insoluble phenol A phenol in which there are substituents on ortho and para positions Unsaturated hydrocarbon (Alkene or alkyne) Aromatic amine Simple water soluble phenol

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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Please help in answering the organic chemistry questions given below. Explanations are welcome.
Question: Explain whether pheromone has geometrical isomers. Draw and label the geometrical isomers, if any. 10 CHIC CH:CHCH CH,CH=CHCOOH
Chemical Name Functional groups present in the molecule Acetaminophen Rank the order of polarity* (1 being the most polar) Aspirin Ibuprofen Naproxen Sodium *The polarity of molecules is ordered as follows, from least to most polar: Alkanes (least polar), alkyl halides, alkenes, aromatic hydrocarbons, ethers, esters, ketones, aldehydes, amines, alcohols, carboxylic acids, amide (most polar).
Complete the following reactions by identifying the major organic product, reagents), or reactant. • If the product is a single compound, draw the structure clearly in the box. • List missing reagents neatly around the blue arrows. There may be more than one reagent per arrow. • If the product is a racemic mixture, clearly draw one enantiomer and write "racemic" under the answer.
When naming disubstituted benzenes, incorporate common names, if possible. Designate the positions of the groups relative to each other by numbering the groups, or by using the designations of ortho, meta, or para Trisubstituted benzenes are named by incorporating common names, if possible. If a common name is used, that group is automatically given the designation of #1. Give the lowest numbering possible. Name each of the following compounds: Br CH3 а. Br b. CI O=N C. Br 16
The second question was incorrect. "The IUPAC nomenclature of benzene compounds primarily will use benzene as the root name. However, common names for substituted benzene compounds exist that use the base names from its derived compounds. The principal functional group will serve as the common root name." Would you mind trying again please? Thank you
CH₂O-C-(CH2) 16CH3 O CHO–C—(CH2) 16CH3 18 O CH₂O-C-(CH2) 16CH3 f. What is the name of the type of functional group that you see in the structure? Write Your Answer Here.
Please don't provide handwriting solution
Part L Give any common name for the following compound. Br CI If the compound has only the IUPAC name, enter no. Submit Request Answer Part J Give any common name for the following compound. Br CH3 If the compound has only the IUPAC name, enter no. 1-bromo-2-methylbenzene Submit Previous Answers Request Answer X Incorrect; Try Again
160. Subject :- Chemistry
Select all of the functional groups that contain rings. ester aldehyde aromatic ring alkane phenol amide alkene thiol ether amine ketone alcohol carboxylic acid cycloalkane Those were the options and I tried many different ones so please provide the accurate ones. I already tried alcohol, aromatic ring, amine, and ether but it was wrong I tried the 3 without aromatic ring and it was also wrong. I tried 6 different ways
What is the structure of molecule A? ( Fenol means phenol) a) Cyclohexylamine b) Aniline c) Benzene d) Anisole e) aminohexane