Polarity: Physical Properties Class Name Polar or pH (Strong or Weak Acid, Neutral, Strong or Weak Base) (Low, High, or HIigh Non polar Solubility with water Boiling Poin (Soluble or Not Soluble) Small structures Large (C1-C4) Structures (C5 or more) Carboxylic Acid Ester Carboxylate Salt Very Polar (But If Carbon chain is long then it has both polar & Nonpolar parts Very Soluble

Polarity: Physical Properties Class Name Polar or pH (Strong or Weak Acid, Neutral, Strong or Weak Base) (Low, High, or HIigh Non polar Solubility with water Boiling Poin (Soluble or Not Soluble) Small structures Large (C1-C4) Structures (C5 or more) Carboxylic Acid Ester Carboxylate Salt Very Polar (But If Carbon chain is long then it has both polar & Nonpolar parts Very Soluble

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

A therapeutic agent (1) can react with sodium hydroxide to produce two new water soluble products. MeO a) (1) COOH Ph Boil with dilute NaOH solution Product A+ Product B Draw the structures of the two products generated from the reaction.
Neutral/acidic/ basic Polar/ non-polar Hydrophobic/hydrophilic
Write or draw the structural formula of each of the following compounds.
Need help with this one: Give at least three (3) specific reactions (ie. with organic reactant's and products and chemical reagents on top of the reaction arrow) for the formation of specific carboxylic acids. Use structures of the reactants and products to show these reactions. No need to give the names for the structures
Draw a reaction showing the reactants (the ester and water) and the products (the alcohol and the carboxylic acid) for each ester below. You can google the structures of the esters. Ester 1 aspirin, Ester 2 benzocaine, Ester 3 gamma-butyrolactone
Draw the line-bond structure of oleic acid (cis-9-octadecenoic acid), CH, (CH₂),CH=CH(CH₂),COOH, at physiological pH. Hydrogen atoms attached to carbon atoms do not need to be drawn. OH
A monobasic acid has a neutralization equivalent of 136+/-1. This acid burns with a sooty flame and gives a negative test for nitrogen, sulfur, and halogens, and is insoluble in water and 5% NaOH. Give a possible structure for this monobasic acid.
Name: Organic Chemistry Nomenclature Project Carboxylic Acids CH, CH, CH OH pentanoic acid H,C- H;C. OH H3C- CH3 CH. 2,5-dimethyl-3-heptenoic acid 4-cyclopropyl-2-nitro-3-butynoic acid он CH 4 methylbut-2-enoic acid OH butadioic acid
Travoprost is a drug used to treat the build-up of pressure in the eye. It is administered as eye drops. HO CF3 ÕH Travoprost (pressure inside the eye, including glaucoma) a) Redraw the structure and incorporate suitable modifications or functional group(s) to: i) increase the polarity of the molecule ii) increase the lipophilicity of the molecule In each case, briefly explain what change(s) you have incorporated and the rationale behind your structural modification. b) Redraw the structure and identify 5 sites that could be targeted by metabolic enzymes, such as cytochrome P450s or transferases. Show two examples of structures arising from potential metabolic activity, using an enzyme or enzymes of your choice.
Draw the skeletal structure of the ester formed when carboxylic acid CH3CH2CH2CH2CO₂H is treated with ethanol (CH3CH₂OH) in the presence of H2SO4 Click and drag to start drawing a structure. G
Please don't provide handwriting solution
Calculate the pH of a 0.0217 M solution of ascorbic acid H₂C6H6O6. The Ka, of ascorbic acid = 5.4 x 10-5 and the Ka, of ascorbic acid = 1.6 x 10-12