ORGANIC CHEMISTRY I PRACTICE PROBLEMS FOR BRONSTED-LOWRY ACID-BASE CHEMISTRY



Similar documents
Chapter 2 - Polar Covalent Bonds; Acids and Bases

Acids and Bases: Molecular Structure and Acidity

Acids and Bases. but we will use the term Lewis acid to denote only those acids to which a bond can be made without breaking another bond

CH 3 CH 2 ONa + H 2 O. CH 3 CH 2 NH 2 + CH 3 OLi

Since we will be dealing with aqueous acid and base solution, first we must examine the behavior of water.

RESONANCE, USING CURVED ARROWS AND ACID-BASE REACTIONS

p3 Recognizing Acid/Base Properties when p11 Recognizing Basic versus Nonbasic

Brønsted-Lowry Acids and Bases

Chapter 16 Acid-Base Equilibria

Chapter 2 Polar Covalent Bonds: Acids and Bases

Acids and Bases: A Brief Review

Write the acid-base equilibria connecting all components in the aqueous solution. Now list all of the species present.

Topic 5. Acid and Bases

MULTIPLE CHOICE QUESTIONS Part 3: Syror och baser (Answers on page 18)

acid: substance which gives up a proton base: substance which accepts a proton

partial positive an acid is a hydrogen ion donor, or proton donor base is a hydrogen ion acceptor, or proton acceptor acidic protons acid base

Chapter 2 Polar Covalent Bonds; Acids and Bases

NH 3 + H 2 O + OH - NH 4. Acid-Base Concepts -- Chapter 15 + H + Conjugate Acid-Base Pairs: - H + base. acid

Chapter 14 - Acids and Bases

An acid is a substance that produces H + (H 3 O + ) Ions in aqueous solution. A base is a substance that produces OH - ions in aqueous solution.

Q.1 Classify the following according to Lewis theory and Brønsted-Lowry theory.

Note: (H 3 O + = hydronium ion = H + = proton) Example: HS - + H 2 O H 3 O + + S 2-

CHAPTERS 15 FAKE TEST QUESTIONS. 1. According to the Brønsted Lowry definition, which species can function both as an acid and as a base?

Titrations. Acid-Base Indicators and Titration Curves. Shapes of Titration Curves. A titration curve is a graphical history of a titration

Chapter 17. How are acids different from bases? Acid Physical properties. Base. Explaining the difference in properties of acids and bases

Electrophilic Aromatic Substitution Reactions

Chapter 9 Lecture Notes: Acids, Bases and Equilibrium

Chapter 19: Acids and Bases Homework Packet (50 pts) Name: Score: / 50

Q.1 Classify the following according to Lewis theory and Brønsted-Lowry theory.

What does pka tell you?

3.4 BRØNSTED LOWRY ACIDS AND BASES

QUESTION (2012:3) (a) (i) Complete the table below showing the conjugate acids and bases. CO 3 H 2 O OH HCN CN -

ACID and BASES - a Summary

Chapter 16: Acid-Base and Solubility Equilibria: Reactions in Soil and Water

Answer Key, Problem Set 5 (With explanations)--complete

Chem 116 POGIL Worksheet - Week 10 - Solutions Weak Acid and Base Equilibria

Acids and Bases. Chapter 16

6) Which compound is manufactured in larger quantities in the U.S. than any other industrial chemical?

Classification of Reagents in Chemistry I: Acids and Bases

Health Science Chemistry I CHEM-1180 Experiment No. 15 Molecular Models (Revised 05/22/2015)

Chapter 14: Acids and Bases

Writing a Correct Mechanism

Acid-Base (Proton-Transfer) Reactions

The strength of the interaction

Section Activity #1: Fill out the following table for biology s most common elements assuming that each atom is neutrally charged.

Name period Unit 9: acid/base equilibrium

AROMATIC COMPOUNDS A STUDENT SHOULD BE ABLE TO:

CHEMISTRY 101 EXAM 3 (FORM B) DR. SIMON NORTH

Nucleophilic Substitution and Elimination

CHAPTER 16: ACIDS AND BASES

Chapter 8 Concepts of Chemical Bonding

Arrhenius Definition. Chapter 15 Acids and Bases. Brønsted-Lowry Concept. Brønsted-Lowry Concept. Conjugate Acid-Base Pairs

Acid-Base Chemistry. Brønsted-Lowry Acids & Bases

Reminder: These notes are meant to supplement, not replace, the textbook and lab manual. Electrophilic Aromatic Substitution notes

Sample Exercise 8.1 Magnitudes of Lattice Energies

ph. Weak acids. A. Introduction


Chapter 17. The best buffer choice for ph 7 is NaH 2 PO 4 /Na 2 HPO 4. 19)

Chem101: General Chemistry Lecture 9 Acids and Bases

Chemistry 201. Practical aspects of buffers. NC State University. Lecture 15

POLAR COVALENT BONDS Ionic compounds form repeating. Covalent compounds form distinct. Consider adding to NaCl(s) vs. H 2 O(s):

Acid Base Titrations in Aqueous Solvents

Acid/base Definitions. Acid/Base Definitions. Acid / Base Chemistry. Acid/Base Definitions. Identifying Acids and Bases

Acid-Base Equilibrium

Chem 112 Intermolecular Forces Chang From the book (10, 12, 14, 16, 18, 20,84,92,94,102,104, 108, 112, 114, 118 and 134)

In the box below, draw the Lewis electron-dot structure for the compound formed from magnesium and oxygen. [Include any charges or partial charges.

1. Oxidation number is 0 for atoms in an element. 3. In compounds, alkalis have oxidation number +1; alkaline earths have oxidation number +2.

ORGANIC CHEM I Practice Questions for Ch. 4

Studying an Organic Reaction. How do we know if a reaction can occur? And if a reaction can occur what do we know about the reaction?

Ch 15: Acids and Bases

Lewis Dot Structures of Atoms and Ions

Which substance contains positive ions immersed in a sea of mobile electrons? A) O2(s) B) Cu(s) C) CuO(s) D) SiO2(s)

Chemistry 1050 Chapter 13 LIQUIDS AND SOLIDS 1. Exercises: 25, 27, 33, 39, 41, 43, 51, 53, 57, 61, 63, 67, 69, 71(a), 73, 75, 79

Electrophilic Aromatic Substitution

Physicochemical Properties of Drugs

Chapter 2: The Chemical Context of Life

Chapter 16 Acid-Base Equilibria. Most solutions that occur in nature are slightly acidic. One reason for this is that when carbon

3/6/2014. Chapter 15. Acids and Bases. Stomach Acid and Heartburn GERD. Curing Heartburn. Common Acids. Properties of Acids. Lecture Presentation

Chapter 6 An Overview of Organic Reactions

4. Acid Base Chemistry

Topic 8 Acids and bases 6 hours

CHAPTER 18 ACID-BASE EQUILIBRIA

Sample Exercise 8.1 Magnitudes of Lattice Energies

Notes on Unit 4 Acids and Bases

Review for Solving ph Problems:

Self Assessment_Ochem I

ACID-BASE REACTIONS/ THE PH CONCEPT.

Acids & Bases. BRONSTED LOWRY ACIDS & BASES A Bronsted Lowry Acid DONATES A PROTON A Bronsted Lowry Base ACCEPTS A PROTON.

How do we determine which molecule is more basic?

Resonance Structures Arrow Pushing Practice

ph: Measurement and Uses

AP*Chemistry The Chemistry of Acids and Bases

A pure covalent bond is an equal sharing of shared electron pair(s) in a bond. A polar covalent bond is an unequal sharing.

Bonding Practice Problems

Unit Two: Acids and Bases

Intermolecular and Ionic Forces

Electrophilic Addition Reactions

Required Reading Material.

Properties of Aqueous Solutions of Acids and Bases. CHAPTER 10 Acids, Bases and Salts. Properties of Aqueous Solutions of Acids and Bases

Mass Spec - Fragmentation

Transcription:

RGANIC CHEMISTRY I PRACTICE PRBLEMS FR BRNSTED-LWRY ACID-BASE CHEMISTRY 1. For each of the species below, identify the most acidic proton and provide the structure of the corresponding conjugate base. You might want to draw detailed Lewis formulas in some cases. HF CH 3 CH 3 CH 3 CH 2 H CH 3 CN H 3 HC CH H 2 H 2 RNH 3 CH 3 H 2 2. For each of the species below, identify the basic atom and provide the structure of the corresponding conjugate acid. You might want to draw detailed Lewis formulas in some cases. S 4 CN _ 2 CH 3 CH 2 H CH 3 CH 2 H PhC H 2 Br NH 2

3. Fill in the reactants or products for the following acid-base reactions. Keep in mind that in line-angle formulas hydrogens are not shown. When in doubt, write complete Lewis structures. Abbreviations used: Ph=phenyl (a benzene ring attached to a carbon chain) HN 3 + H 2 F + H 3 H 3 C CH 3 + H PhC + HCl H 2 C 3 + H + H 2 NH 3 + HC C H + H 4. Arrange the substances by order of acidity or basicity as indicated. You may use pka tables, periodic tables, or any other tools available to you (except for your cell phone). H 2 Se H 2 H 2 S Br F I Cl strongest base weakest base CH 4 HI PH 3 H 2 Se F H NH 2 CH 3 CH 2 CH 2 CH 2 weakest basse strongest base CH 3 CH 2 H CH 3 CH HF Benzene

5. Circle the side favored by equilibrium in the following acid-base reactions. CN + NH 3 HCN + NH 2 H + H3 C CH 2 + H3 C CH 3 H 2 + NH 3 H 3 + NH 2 H 2 C 3 + H 2 HC 3 + H 3 CH 3 CH 2 CH 2 CH 3 + CH 2 CH 3 CH 2 CH 2 CH 2 + CH 3 6. The conjugate acid of ammonia, NH 3, is: A) NH 4 + B) NH 2 H C) NH 2 - D) none of the above 7. Methanesulfonic acid, CH 3 S 3 H, has a pk a of -7 while ethanol, CH 3 CH 2 H, has a pk a of 15.9. Which is the stronger acid and what accounts for this large difference in relative acidity? 8. Would you predict trifluoromethanesulfonic acid, CF 3 S 3 H, to be a stronger or weaker acid than methanesulfonic acid, CH 3 S 3 H? Explain your reasoning. 9. Consider the species CH 3 -, NH 2 -, and CH 3 C-. Rank these ions in order of increasing basicity, and explain your rationale. 10. The K a of formic acid is 1.7 x 10-4. The pk a of formic acid is. A) 1.7 B) 10.3 C) 4.0 D) 3.8 E) -2.3 11. Provide the structure of the conjugate base of phenol (shown below) and all its resonance forms. H 12. Rank the following in order of increasing acidity: CH 3 H, HCl, NH 3, and CH 4. 13. Rank the following in order of increasing basicity: CH 3 -, H 2 N -, H 2, and NH 3.

14. When methanol (CH 3 H) acts as a base, its conjugate acid is. A) CH 4 H B) CH 3 H + 2 C) CH 4 + D) CH 3 - E) - CH 2 H 15. Which of the following pairs of bases lists the stronger base first? A) H 2 > H - B) H 2 N - > CH 3 C - C) CH 3 C - > H - D) I - > Cl - E) H - > H 2 N - 16. Draw the structure of the conjugate acid of acetone (CH 3 CCH 3 ).

ANSWERS 1. HF F CH 3 CH 3 CH 3 CH 2 CH 3 CH 2 H CH 3 CH 3 CH 3 CN CH 2 CN H 3 H 2 HC CH HC C H 2 H H 2 H RNH 3 RNH 2 CH 3 H 2 CH 3 H 2. CN HCN CH 3 CH 3 CH 3 CH 2 H S 4 _ 2 HS 4 H H 2 CH 3 CH 2 H CH 3 CH 2 H 2 PhC PhCH H 2 H 3 Br HBr NH 2 NH 3

3. HN 3 + H 2 H 3 + N 3 HF + H 2 F + H 3 + H + H 2 H 3 C CH 3 H 3 C CH 2 PhCH + Cl PhC + HCl H 2 C 3 + H HC 3 + H 2 + H 2 + H NH 2 + HC CH NH 3 + HC C H + H + H 2 4. Periodic trend H 2 < H 2 S < H 2 Se Periodic trend F strongest base > Cl > Br > I weakest base Periodic trend HI > H 2 Se > PH 3 > CH 4 Periodic trend F < H < NH 2 < CH 3 CH 2 CH 2 CH 2 weakest basse strongest base pk a trend Benzene < CH 3 CH 2 H < CH 3 CH < HF

5. The numbers represent approximate pk a values for the substances acting as acids. CN + NH 3 HCN + NH 2 38 9 H + H3 C CH 2 + H3 C CH 3 17 20 H 2 + NH 3 H 3 + NH 2 4-1.7 H 2 C 3 + H 2 HC 3 + H 3 6.4-1.7 CH 3 CH 2 CH 2 CH 3 + CH 2 CH 3 CH 2 CH 2 CH 2 + CH 3 48 40 6. A 7. Methanesulfonic acid is the stronger acid. The lower the pka, the stronger the acid. A lower pka is associated with a larger Ka which signifies greater dissociation. The large relative difference in acidity in this case can be most easily seen by gauging the relative basicities of the conjugate bases. The weaker the base, the stronger the corresponding conjugate acid. Methanesulfonate, CH 3 S 3 -, is considerably stabilized by resonance delocalization which is not found in ethoxide, CH 3 CH 2 -. This effect greatly reduces the basicity of methanesulfonate relative to ethoxide. Draw the Lewis formula for methanesulfonate and the resonance forms for practice. 8. Trifluoromethanesulfonic acid is a stronger acid. Compare the strengths of the conjugate bases and remember that the weaker the base, the stronger the conjugate acid. Both bases are stabilized by resonance, but in the case of the trifluoro derivative, the presence of the highly electronegative fluorine atoms serves to delocalize the negative charge to an even greater extent by the inductive effect of fluorine. This additional delocalization makes trifluoromethanesulfonate a weaker base. 9. CH 3 C- < CH 3 - < NH 2 - first factor to consider is the nature of the atom which bears the negative charge. The more electronegative the atom that bears the negative charge, the more stable the

anion. Stable anions are less reactive and are hence weaker bases. Since is more electronegative than N, the NH 2 - is the strongest base in the set. In the remaining two species, the negative charge is on the, but in the case of CH 3 C-, the negative charge is also delocalized by resonance. 10. D 11. See class notes, or p. 417 of the Wade textbook, for all the resonance structures of the phenoxide ion shown below. (see p. 429 for 4 more resonance resonance structures) structures 12. CH 4 < NH 3 < CH 3 H < HCl (periodic trend) 13. H 2 < NH 3 < CH 3 - < H 2 N - Negatively charged ions are stronger bases than neutral counterparts. A table of pk a values will further aid in deciding the final order of basicity. 14. B 15. B 16. H H 3 C CH 3