A. REACTIONS OF HYDROCARBONS Three hydrocarbon samples were analyzed by various qualitative tests and the summary of their reactions is given in Table 1 below. Identify each unknown sample by matching the respective reaction profile with the given structures (A, B, or C). Table 1. Summary of Reactions of Hydrocarbon Samples Sample Brz in CCI4 KMNO, in NaOH AGNO; in NH; Fading of reddish- brown color Brown precipitates 1 No reaction Fading of reddish- brown color Brown precipitates Silver precipitates Fading of reddish- brown color No reaction No reaction CH H3C CH3 H,C ČH3 A C Sample Identity and Rationalization 1 3

A. REACTIONS OF HYDROCARBONS Three hydrocarbon samples were analyzed by various qualitative tests and the summary of their reactions is given in Table 1 below. Identify each unknown sample by matching the respective reaction profile with the given structures (A, B, or C). Table 1. Summary of Reactions of Hydrocarbon Samples Sample Brz in CCI4 KMNO, in NaOH AGNO; in NH; Fading of reddish- brown color Brown precipitates 1 No reaction Fading of reddish- brown color Brown precipitates Silver precipitates Fading of reddish- brown color No reaction No reaction CH H3C CH3 H,C ČH3 A C Sample Identity and Rationalization 1 3

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter4: Polar Bonds, Polar Reactions

Section: Chapter Questions

Problem 4E

See similar textbooks

Similar questions

Using the following chemical analyses below, obtain the probable structure of the following hydrocarbon compound. Provide probable structure of the compound. Provide a probable structure of the compound. Support using the chemical structures obtained from the ozonolysis, hydroboration-oxidation, and hydrogenetion.
1. Write three major criteria of forming a Hydrogen bond in bullet points with example. 2. Certain amount of pure charcoal (carbon) has to be burnt with supplied natural air. Process engineer allowed the exact amount of air required to burn the entire charcoal completely to carbon dioxide. Carbon has no reaction with nitrogen gas present in the air. In the reaction outlet if 5 kg of nitrogen gas was found, calculate the amount of charcoal used. (12C, 16O, 14N)
prepare glyoxal from acetylene and acetylene from tetrahalide and carbon tetrachloride from methane with explaination
On the two structures , choose a structure that is highly unfavoured andexplain why that structure is not favoured
3) Enols are an important class of molecules in organic chemistry, which are utilized for theirability to form carbon-carbon bonds. We will learn about their unique reactivity much later inthe course. Shown below is an enol on the left, whereas the molecule on the right is classifiedas an allylic alcohol. a) Please explain why the structure on the right IS NOT a resonance structure of the enol on theleft. A short statement or illustration is fine, be sure that your rationale is clear. b) Draw the correct resonance structure that can be produced from the enol on the left. Besure to include arrows to indicate the movement of electrons in the left-hand structure andindicate charges in the resulting structure. c) What is the hybridization of the carbon indicated with the red arrow?
Help with the following ochem reaction scheme... Consider 3,4-dimethylpiperidine being subjected to the below reaction scheme: step 1) CH3I (excess) step 2) NaOH, heat step 3) CH3I (excess) step 4) NaOH, heat Provide the bond line structures for the major organic product obtained in each step and then discuss the regiochemistry for step 2.
please don't provide handwrittin solution.. What is name of this structure? Give explantion and steps for supporting.
In the reactions given below, write to which organic molecule Y, Z, T, A ‘belongs, and give information about the reaction types that take place.
Give a clear handwritten answer...give the missing products and regents of given sub parts reactions
A compound of formula C6H10 takes up 1 mole of H2 on reduction. Give one possible structure that would fit the information.
An unknown hydrocarbon G, whose formula is C16H26 contains two triple bonds. Ozonolysis followed by reduction with (CH3)2S gave CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. Suggest a reasonable structure for compound G.
1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above 2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10 3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above 4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2 5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the above