2 An unknown compound X can be one the three compounds listed in the table below. A mixture of X with 4-chlorophenylacetic acid melts at 95-102 °C, a mixture of X with oxalic acid melts at 93- 101°C, and a mixture of X with 2-methylbenzoic acid melts at 103-105 °C. Give the nature of X Oxalic acid 101-102 °C D 4-chlorophenylacetic acid 104-105 °C 2-methylbenzoic acid 103-105 °C none of the above

2 An unknown compound X can be one the three compounds listed in the table below. A mixture of X with 4-chlorophenylacetic acid melts at 95-102 °C, a mixture of X with oxalic acid melts at 93- 101°C, and a mixture of X with 2-methylbenzoic acid melts at 103-105 °C. Give the nature of X Oxalic acid 101-102 °C D 4-chlorophenylacetic acid 104-105 °C 2-methylbenzoic acid 103-105 °C none of the above

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

Give the systematic (IUPAC) names for these molecules. Boononon cnolonongron. НаСНз CHОССH2СH2СНCHЗ CH3 phenyl propanoate |4-methyl pentane methanoat Incorrect. You mixed up the acyl and alkoxy portions of the molecule. Name the alkoxy part first, followed by the acyl part.
Please don't provide hand written solution
The substance N,N-dimethylaniline is a weak nitrogenous base like ammonia. Complete the following equation that shows how N,N-dimethylaniline reacts when dissolved in water. -N(CH3)2 + ? CH3 -ŃCH3 +
An unknown compound is treated with peroxyacetic acid in dilute sulfuric acid. The product of reaction 1 is reacted with excess PBr3 , then excess NaNH2 (reaction 3). The product of reaction 3 is treated with lithium, then n-butylbromide (reaction 4). In reaction 5 the product of reaction 4 is reacted with ozone, then NaHSO3. This final reaction produced 2 acids, propanoic acid and pentanoic acid. What was the original unknown compouond?
Give the name of the product formed when hydrochloric acid is mixed with N,N-dimethyl-2-propanamine.
The substance N,N-dimethylaniline is a weak nitrogenous base like ammonia. Complete the following equation that shows how N,N-dimethylaniline reacts when dissolved in water. -N(CH₂)2 + ? CH3 +
Draw the structural formulas of the following compounds, name them according to IUPAC (1,2,3,4,5,6 examples), indicate the asymmetric carbon atoms. 5) γ-hydroxyvaleric acid 6) δ-hydroxyvaleric acid 7) 2-hydroxypentanoic acid 8) 3-hydroxy-2-methylbutanoic acid 9) 2,3- dihydroxybutanedioic acid (tartaric acid)
An unknown compound is treated with peroxyacetic acid in dilute sulfuric acid. The product of reaction 1 is reacted with excess PBr3 , then excess NaNH2 (reaction 3). The product of reaction 3 is treated with lithium, then n-butylbromide (reaction 4). In reaction 5 the product of reaction 4 is reacted with ozone, then NaHSO3. This final reaction produced 2 acids, propanoic acid and pentanoic acid. What was the original unknown compouond?
The phospholipid structure shown above provides for ___? The hydrophobic by-layer of cell membranes The hydrophilic inner and outer surfaces of cell membranes a and b