Homework Answers
Polar and non polar nature of the compoud is decided based the electronegativity difference between the bonded atoms.
ionic compounds are polar and polar compouds have greter electronegativity difference between bonded atoms.
The bond between same atoms is nonpolar. In Non polar copoundes the bondeded aotms have nearly same electronegativity.
Ethylele glycol POLAR.
Oil NONPOLAR
Biphenyl NONPOLAR
Hexane NONPOLAR
Sugar POLAR
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Referring to Parts A & B in the experiment, indicate whether the following compounds are polar...
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of...
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of the intermolecular forces that would occur between the molecules of acetone and the molecules of 2- propanone if you have a mixture of the two liquids. What would be the main type of IMF that is responsible for the attraction? (Give a name for the IMF). c). The pentane molecule and the 2-pentanone molecule both have five carbon atoms on their structures. Why 2-pentanone...
I. Nylon 6-6 is a condensation polymer. The last two lab handouts pointed out that "condensation...
I. Nylon 6-6 is a condensation polymer. The last two lab handouts pointed out that "condensation reactions are extremely common among a variety of organic functional groups." Pick two appropriate functional groups (your choice) and draw structures to show the condensation reaction between them. Identify the functional groups that are reacting, as well as the linkage formed by the condensation. 2. Rather than use a carboxylic acid for the nylon condensation, you'll use the more reactive acid chloride. This must...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate the hydrogen bonds with dotted lines. :N-CEN: H 10. Polar molecules can contain more than one type of attractive force. Fill in the following table answering the question "Is this attractive force present between molecules of the given compound?" Write yes or no for each force. Molecule Ionic Attraction H-Bond Dipole-Dipole London CHCl3 CH3OH NH2 65- *NH3-C-COO 11. For each of the following pairs...
PART IV. MISCIBILITY OF TWO LIQUIDS 1. For the first two liquids in Table IV-B (the...
PART IV. MISCIBILITY OF TWO LIQUIDS
1. For the first two liquids in Table IV-B (the solvents in the
miscibility tests), use the molecular structures provided in the
Introduction to identify each liquid as polar or nonpolar. Put an X
in the appropriate column.
2. For the remaining liquids in Table IV-B, determine if they
are primarily polar, primarily nonpolar, or both polar and polar
based on your observations in Table III-A and based on the polarity
of the solvent....
2. Identify the strongest type of intermolecular forces in acetone, ethanol, water and hexane. (Structures listed...
2. Identify the strongest type of intermolecular forces in acetone, ethanol, water and hexane. (Structures listed on page 15.) Experiment 2 Intermolecular Forces There are three general types of intermolecular forces. All substances exhibit London Dispersion Forces (LDF), and they are generally the weakest of the three types. These London forces are due to the attractions between small, temporary dipoles that arise from the constant, random movement of the electrons in a substance. As molar mass increases, the size of...
Tools Window Help OMX 75% Esterification Experiment Lab Data.pdf (page 1 of 3) Search Product Ester...
Tools Window Help OMX 75% Esterification Experiment Lab Data.pdf (page 1 of 3) Search Product Ester IR of starting alcohol (1-pentanol) 1-Pentanol M. AM 19ra aromo 14, 2017 m. 1% 1075 20 . 2030 26.1.60.39 10 4000 3500 . 1000 3000 INT 650 2500 cm-1 2000 1500 M 8 Tools Window Help 78 Wed 2:19 PM Go Esterification Experiment Lab Data pdf page 2 of 3) @ Q Search IR of final product (ester) Product Ester Guided Instructions for In-Lab...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.)...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
i need help answering these qoustion plz???? Use the short grey sticks for single bonds and...
i need help answering these qoustion plz????
Use the short grey sticks for single bonds and the long flexible grey sticks for double and triple bonds. Note: In reality, single bonds are longer than double or triple bonds ) Fill in the table below Molecule # of lone pairs on central atom linear or bent? (Circle one) HO lincar benti SO lincar bent CO. bent lincar HCN bent lincar Question: Based on your answers in the table above and the...
if applicacable, please write clear stepwise mechanism for all synthetic transformations, showing important internediates where appropriate....
if applicacable, please write clear stepwise mechanism for all
synthetic transformations, showing important internediates where
appropriate. only do this if applicable for this lab.
Experiment SD Column Chromatography Running the Reaction. Once sodium borohydride has been added to the reaction meture Isee next paragraph take samples at the times just indicated. Because this must be done in such a short time you must be well prepared before starting the reaction. One person should be the timekeeper, and the other person...
Exercise 2 Separation of a Mixture Based on Acid-Base Properties One purpose of this exercise is...
Exercise 2 Separation of a Mixture Based on Acid-Base Properties One purpose of this exercise is to learn how to use a separatory funnel to extract a single component away from other compounds in solution. To do so, we will apply the principles of solubility and acid-base behavior you’re seeing in class. One of the compounds is neutral in the acid-base sense. It has no ability to either donate or accept a proton from an aqueous solution, and will remain...
7). a). Is the acetone molecule non-polar or polar? Circle. Non-polar Polar b). Sketch pictures of the intermolecular forces that would occur between the molecules of acetone and the molecules of 2- propanone if you have a mixture of the two liquids. What would be the main type of IMF that is responsible for the attraction? (Give a name for the IMF). c). The pentane molecule and the 2-pentanone molecule both have five carbon atoms on their structures. Why 2-pentanone...
I. Nylon 6-6 is a condensation polymer. The last two lab handouts pointed out that "condensation reactions are extremely common among a variety of organic functional groups." Pick two appropriate functional groups (your choice) and draw structures to show the condensation reaction between them. Identify the functional groups that are reacting, as well as the linkage formed by the condensation. 2. Rather than use a carboxylic acid for the nylon condensation, you'll use the more reactive acid chloride. This must...
9. Draw all of the possible hydrogen bonds between the following molecule and water molecules. Indicate the hydrogen bonds with dotted lines. :N-CEN: H 10. Polar molecules can contain more than one type of attractive force. Fill in the following table answering the question "Is this attractive force present between molecules of the given compound?" Write yes or no for each force. Molecule Ionic Attraction H-Bond Dipole-Dipole London CHCl3 CH3OH NH2 65- *NH3-C-COO 11. For each of the following pairs...
PART IV. MISCIBILITY OF TWO LIQUIDS
1. For the first two liquids in Table IV-B (the solvents in the
miscibility tests), use the molecular structures provided in the
Introduction to identify each liquid as polar or nonpolar. Put an X
in the appropriate column.
2. For the remaining liquids in Table IV-B, determine if they
are primarily polar, primarily nonpolar, or both polar and polar
based on your observations in Table III-A and based on the polarity
of the solvent....
2. Identify the strongest type of intermolecular forces in acetone, ethanol, water and hexane. (Structures listed on page 15.) Experiment 2 Intermolecular Forces There are three general types of intermolecular forces. All substances exhibit London Dispersion Forces (LDF), and they are generally the weakest of the three types. These London forces are due to the attractions between small, temporary dipoles that arise from the constant, random movement of the electrons in a substance. As molar mass increases, the size of...
Tools Window Help OMX 75% Esterification Experiment Lab Data.pdf (page 1 of 3) Search Product Ester IR of starting alcohol (1-pentanol) 1-Pentanol M. AM 19ra aromo 14, 2017 m. 1% 1075 20 . 2030 26.1.60.39 10 4000 3500 . 1000 3000 INT 650 2500 cm-1 2000 1500 M 8 Tools Window Help 78 Wed 2:19 PM Go Esterification Experiment Lab Data pdf page 2 of 3) @ Q Search IR of final product (ester) Product Ester Guided Instructions for In-Lab...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
i need help answering these qoustion plz????
Use the short grey sticks for single bonds and the long flexible grey sticks for double and triple bonds. Note: In reality, single bonds are longer than double or triple bonds ) Fill in the table below Molecule # of lone pairs on central atom linear or bent? (Circle one) HO lincar benti SO lincar bent CO. bent lincar HCN bent lincar Question: Based on your answers in the table above and the...
if applicacable, please write clear stepwise mechanism for all
synthetic transformations, showing important internediates where
appropriate. only do this if applicable for this lab.
Experiment SD Column Chromatography Running the Reaction. Once sodium borohydride has been added to the reaction meture Isee next paragraph take samples at the times just indicated. Because this must be done in such a short time you must be well prepared before starting the reaction. One person should be the timekeeper, and the other person...
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