Inorganic Chemistry with Doc M. Day 10. Ionic Thrills, Part 1.

Similar documents
Inorganic Chemistry with Doc M. Fall Semester, 2012 Day 13. Ionic Thrills Part 3.

These metal centres interact through metallic bonding

Chapter 1. Crystal Structure


METALLIC CRYSTALS. tend to be densely packed. have several reasons for dense packing: have the simplest crystal structures.

Unit-1 THE SOLID STATE QUESTIONS VSA QUESTIONS (1 - MARK QUESTIONS)

SOLID-STATE STRUCTURE.. FUNDAMENTALS

3. [7 points] How many significant figures should there be in the answer to the following problem?

Order in materials. Making Solid Stuff. Primary Bonds Summary. How do they arrange themselves? Results from atomic bonding. What are they?

CRYSTAL STRUCTURE TERMS

Solids. The difference between crystalline and non-crystalline materials is in the extent of ordering

Stacking Oranges. Packing atoms together Long Range Order. What controls the nearest number of atoms? Hard Sphere Model. Hard Sphere Model.

Chapter 13 THE GROUP 13 ELEMENTS. Exercises

INTERPRETING CHEMICAL FORMULAS AND SYMBOLS

Topic: Bargg Equation

CHAPTER. The Structure of Crystalline Solids

Chapter 17 Solubility and Complex Ion Equilibria

CH445/545 Winter 2008

Metallic crystal structures The atomic bonding is metallic and thus non-directional in nature

(C) Na 2. (B) NaWO 3 WO 3

Chem 253, UC, Berkeley. Chem 253, UC, Berkeley

Chapter 3: Atomic and Ionic Arrangements. Chapter 3: Atomic and Ionic Arrangements Cengage Learning Engineering. All Rights Reserved.

CHAPTER THE SOLID STATE

Crystal structure of the material :- the manner in which atoms, ions, or molecules are spatially.

KEY FIRST MIDTERM EXAM Chemistry February 2009 Professor Buhro

2.4 Period 3. Na Mg Al Si P S Cl Ar

Sn 2+ (aq) + 2 Ag + (aq) Sn 4+ (aq) + 2 Ag(s),

Intermolecular Forces. Part 2 The Solid State: Crystals

Fundamental concepts and language Unit cells Crystal structures! Face-centered cubic! Body-centered cubic! Hexagonal close-packed Close packed

FIRST MIDTERM EXAM Chemistry March 2011 Professor Buhro

Class XII Chapter 1 The Solid State Chemistry

Chapter 12: Intermolecular Forces and Liquids and Solids

1.10 Close packed structures cubic and hexagonal close packing

Neighbour s envy, Owner s pride, Silicon Valley s delight, a girl s best friend, Miner s blackjack! Is that you?

CHM101 SECOND EXAM 162. Chemistry 101 SECOND Exam (162) Name: Date: 30/4/2017

1. Which of the given statements about the reaction below are incorrect?

Diffusion & Crystal Structure

NPTEL COURSE ADVANCED CERAMICS FOR STRATEGIC APPLICATIONS QUESTIONS AND ANSWERS

Unit 1 The Solid State

21. sodium nitrite 31. potassium carbonate. 23. aluminum hydroxide 33. nickel (II) carbonate. 24. ammonium hydroxide 34.

Chemistry/Materials Science and Engineering C150 Introduction to Materials Chemistry

CHEM 200/202. Professor Gregory P. Holland Office: GMCS-213C. All s are to be sent to:

9.2.1 Similarities and trends in the properties of the Group II metals magnesium to barium and their compounds

Chem 241. Lecture 19. UMass Amherst Biochemistry... Teaching Initiative

Name: Date: Period: Page: Predicting Products. Predict the products, and balance each reaction. Use the reaction type as a hint.

General Characteristics of Solid State

Chapter Outline. How do atoms arrange themselves to form solids?

Chapter Outline How do atoms arrange themselves to form solids?

Exercise 6a. Balancing equations

Summer Assignment Coversheet

Balance the following equations: 1. Al + N 2 AlN. 2. Fe + O 2 Fe 3 O CaCO 3 CaO + CO 2 4. NH 4 NO 3 N 2 O + H 2 O. 5. KI + Cl 2 KCl + I 2

Close Packings of Spheres I.

CHAPTER 2: ATOMIC ARRANGEMENTS AND MINERALOGICAL STRUCTURES. Sarah Lambart

Chapter 9 Systematic Equilibrium

AP Chemistry A. Allan Chapter 18 - The Representative Elements: Groups 1A through 4A

Chapter 16. Liquids and Solids. Chapter 16 Slide 1 of 87

Chapter 11. States of Matter Liquids and Solids. Enthalpy of Phase Change

Part 1. References: Gray: Chapter 6 OGN: Chapter 19 and (24.1)

SECOND MIDTERM EXAM Chemistry April 2011 Professor Buhro

Chem : Feb E3 Redox: Transferring Electrons. E3: Redox: Transferring Electrons

Semiconductors. Types of Solids. Figure 10.30: Energy-level diagrams for (a) an n-type semiconductor and (b) a ptype semiconductor.

Thermal decomposition. Metal carbonates

LAB II CRYSTAL STRUCTURE AND CRYSTAL GROWTH PART 1: CRYSTAL GROWTH. I. Introduction

Lecture 3: Description crystal structures / Defects

Chapter 12 Metals. crystalline, in which particles are in highly ordered arrangement. (Have MP.)

PO 4 NH 4 H + + SO 3

Name: Mods: Date Agenda Homework

Electrochemistry Written Response

Chemistry 145 Exam number 4 name 11/19/98 # Faraday s constant is 96,500 c/mole of electrons.

1. Name the first element by its name. 2. The second element has the ending ide. 3. The number of atoms of each element is indicated with Greek

Chem : Oct. 1 - Oct. 7

Point Defects in Metals

SNC 2D0-01 Chemistry Review Chapters 5 and 6

CHAPTER 5 IMPERFECTIONS IN SOLIDS PROBLEM SOLUTIONS

SOLUBILITY STUDY GUIDE- Multiple Choice Section

CHAPTER 3: CRYSTAL STRUCTURES & PROPERTIES

Today! Demonstrations of Redox Chemistry! Electrochemistry! electrons moving about! equilibrium with a control knob! The disappearing Aluminum Rod!

Crystal Structures of Interest

Chem : Feb.12-17

Topic Reacting masses Level GCSE Outcomes 1. To calculate reacting masses 2. To set out mole calculations in a grid format

ENGINEERING MATERIALS LECTURE #4

Chemistry. TOPIC : Redox Reactions. products are PH3 and NaH2PO2. This reaction is an examplee of. (b) Reduction (d) Neutralization

Materials Science ME 274. Dr Yehia M. Youssef. Materials Science. Copyright YM Youssef, 4-Oct-10

Packing of atoms in solids

TYPES OF CHEMICAL REACTIONS PART I INTRODUCTION

Ceramic Science 4RO3. Lecture 2. Tannaz Javadi. September 16, 2013

NOMENCLATURE (ie naming compounds)

Please write the balanced net ionic reaction for each one. Then answer the accompanying question.

The s-block elements: Alkali and alkaline earth metals

MAIN GROUPS CHEMISTRY. Alkaline Earth Metals ( Group IIA)

1. Nickel has a face-centered-cubic unit cell. The density of nickel is 6.84 g/cm 3. Calculate the atomic radius of nickel.

Chapter 12: Structures & Properties of Ceramics

Combination Reactions 2H 2 + O 2 2H 2 O. 2Na + I 2 2NaI. Ca + Cl 2 CaCl 2. C + O 2 CO 2 or 2C + O 2 2CO 3H 2 + N 2 2NH 3

[ Cl ] - [[Mg 2+ ] ] Experiment 7: Oxidation-Reduction Reactions. transfer e -

1. What volume of water is required to make a 4.65 M solution from 5.2 g of NaBr (MM = g/mol)?

Chapter 18 Homework Answers

Structure of silica glasses (Chapter 12)

Chapter 10. Liquids and Solids

Properties of II B Group Elements

85 Q.14 In which of the following substances does nitrogen have the lowest oxidation number?

Transcription:

Inorganic Chemistry with Doc M. Day 10. Ionic Thrills, Part 1. Topics: 1. Properties of ionic substances 7. Octahedral and tetrahedral holes 2. Cubic lattices and the periodic table 8. The cesium chloride lattice 3. Simple cubic unit cell 9. The fluorite lattice 4. Face-centered unit cell 10. The zinc blende lattice 5. Body-centered unit cell 11. Diamond 6. Sodium chloride lattice 1. Properties of Ionic Substances (a) List properties of ionic compounds. (b) How would one identify a compound as either ionic or covalent? 2. Cubic lattice structures and the periodic table. A number of metals exist in one of the cubic lattice types. The three cubic lattices are simple cubic, face-centered cubic and body-centered cubic. Day 10 Ionics 1 1

3. The simple cubic unit cell. (a) Sketch in the atoms for a simple cube. Example: polonium (b) Where do the atoms come into contact with one another? Show this on the front view (above right). (c) How many atoms are present per unit cell? Show work. (d) How does the atomic radius, r, compare to the unit cell edge length, e? Solve for e. (e) What is the formula for volume in terms of r? (f) What percent of the space in the unit cell is occupied? Report this as a number. Day 10 Ionics 1 2

4. The face-centered cube (examples: Al, Ca, Ni, Cu, Ge, Sr, Rh, Pd, Ag) (a) The fcc lattice allows atoms to be close-packed (as densely packed as possible more on this later.) The atoms of the fcc structure make contact along the face-diagonals as shown above right. Sketch in the atoms for a face-centered cube on the cubic unit cell templates above use small circles in the figure at left so that the locations can be seen and large space-filling circles in the front view (above right) to show where the atoms come into contact with one another. (b) How many atoms are present per unit cell? Show work. (c) How does the atomic radius, r, compare to the unit cell edge length, e? Solve for e. (d) What is the formula for volume in terms of r? (e) What percent of the space in the unit cell is occupied? Report this as a number. (f) Calcium exists in the fcc lattice. Given that the atomic radius of metallic calcium is 197 pm, calculate the volume of a unit cell of calcium in cm 3. Day 10 Ionics 1 3

(g) Determine the density of calcium and compare your results with the known density, 1.54 g/cm 3. (h) Determine the density of calcium erroneously assuming it exhibited a simple cube lattice and compare your results with the known density, 1.54 g/cm 3. 5. The body-centered Cube (a) Sketch in the atoms for a body-centered cube (examples: All Group I, Ba, V, Cr, Mn, Fe, Nb, Mo, W) (b) Where do the atoms come into contact with one another? (c) How many atoms are present per unit cell? Show work. Day 10 Ionics 1 4

(d) How does the atomic radius, r, compare to the unit cell edge length, e? Solve for e. (e) What is the formula for volume in terms of r? (f) What percent of the space in the unit cell is occupied? Report this as a number. 6. The sodium chloride lattice. (MANY ionic compounds have this structure including all of the alkaline earth oxides, e.g. MgO, SrO). (a) In the case of NaCl, which ions are the large spheres and which are the small ones? (b) The anions and cations each form a lattice of their own called a sub-lattice. What is the sublattice of anions? (c) Sketch the NaCl lattice on the template (right) placing the anions so that they are on the corners of the cube. (d) Locations within all unit cells have names, most of which you already know, such as corner, facecenter, body center. Another position is the edgecenter. From its name, you should be able to describe the location of the edge-center positions. How many edge-centered positions are there in the fcc unit cell? Day 10 Ionics 1 5

(e) Edge-centered positions are only partially inside each a particular unit cell. What fraction of each edge-centered position is in any given unit cell? Multiply by the number of edge-centered positions determined above and you have the total maximum occupancy for ions using edge-centered positions. What is this number? (f) In the case of NaCl, the unit cell is thought of in terms of the sub-lattice chloride ions, perhaps because they are largest. From that perspective, most of the Na + cations occupy the edge-centers of the unit cell. There is one more sodium cation that is not on an edge-centered position. Where is it? (g) Summarize what we have learned so far by completing the rest of the table. Corner positions 8 x 1 / 8 = 1 Face-centered positions 6 x 1 / 2 = 3 Body-centered positions 1 x 1 = 1 Simple cube Yes No Edge-centered positions 12 x 1 / 4 = 3 Face-centered cube Body-centered cube Yes Yes NaCl lattice Chlorides Sodium cations (h) What is the ratio of Cl - to Na + in the unit cell? How does this compare to its formula? (i) The Na + ion has a radius of 116 pm and the Cl - ion has a radius of 167 pm. Determine the length of the edge, e, and the volume, V, of the unit cell (in cm 3 ). (j) Predict the density of NaCl and compare it to the actual value, 2.165 g/cm 3. Day 10 Ionics 1 6

7. Octahedral and tetrahedral holes. Close-packed unit cells include the fcc and the hexagonal close-packed (hcp) unit cells we have not yet discussed the hcp unit cell. Both fcc and hcp have the large ions (or neutral atoms) arranged in a close-packed arrangement (there is no more efficient way to pack these spheres.) Yet, between the spheres, there are open spaces. Upon closer inspection, these holes are one of only two types. There are larger holes defined as the space created by six of the large spheres all equally distant from the center of the hole these are called octahedral holes. Copy your work from the top of page 3 here and identify the octahedral holes by marking them with O. All together, you should find 13 locations for octahedral holes. There are smaller holes defined as the space created by the space created by four of the large spheres all equally distant from the center of the hole called tetrahedral holes. The location of one of these holes is shown two different ways in the figures below. The Cartesian coordinates shown in the figure on the left only indicate the center of the tetrahedral hole. How many tetrahedral holes are present within a fcc unit cell? (b) Determine the ratio of spheres : octahedral holes : tetrahedral holes fully contained within the fcc unit cell. Day 10 Ionics 1 7

(c) Using four spheres, place three of them in mutual contact a plane of three spheres that make an equilateral triangle shape the C 3 face of a tetrahedron. Sketch this below. Place the fourth sphere on a second layer above the first three and resting in the divot of the three touching spheres. Imagine a much smaller sphere in the tiny 4-sided, 3- dimensional hole created by the four spheres. You have created a tetrahedral hole. (d). Let s return to the NaCl lattice. Each sodium cation is in an octahedral hole. What are the closest neighbors of each sodium cation? How many nearest neighbors does each ion in NaCl have? 8. The cesium chloride lattice. The CsCl lattice is usually encountered when we have cations that are similar in radius to the anions. Both anion and cation sub-lattices form a simple cube, however one sub-lattice is offset by one-half the edge distance in all three dimensions (that is to say that the cation sublattice occupies the body-centered positions of the anion sublattice (or visa versa). (a) Sketch the CsCl lattice on this template placing the anions so that they are on the corners of the cube. (b) Complete the following table for NaCl and CsCl. Write either Na + (or Cs + ) or Cl -. Corner Face-center Body-center Edge-center NaCl CsCl Day 10 Ionics 1 8

(c) What sub-lattices does Cl - have in the CsCl structure? (d) What is the ratio of Cs + to Cl - in the unit cell? How does this compare to its formula? (e) What is the coordination number for Cs + and Cl - in the CsCl structure? What is the coordination number for Na + and Cl - in the NaCl structure? (f) The density of CsCl is 3.988 g/cm 3. Knowing that density = mass/volume, determine the volume of the CsCl unit cell and use that value to determine the length of an edge, e, in units of pm. (g) Continuing on, use the value for the edge, e, to determine the diagonal length from one corner to the opposite corner of the cube. This distance equals 2 x r Cs + + 2 x r Cl -. Given the ionic radius for Cs + ion is 188 pm, calculate the r Cl - in pm. Day 10 Ionics 1 9

9. The fluorite lattice. Fluorite is CaF 2. There are two equivalent ways to think about the fluorite structure. (a) The fluorides form a simple cubic lattice. Sketch eight unit cells worth of fluorides on the template provided at left, below (b) The calcium cations exist in alternating body-center positions. Sketch them in. (c) What is the coordination number (number of nearest neighbors of opposite charge) for each ion? (d) The other way to think about the fluorite structure is to think of a fcc of calcium ions (Ca +2 has slightly larger radius than F - ) with the fluorides in all of the tetrahedral holes. Sketch this on the right template, above. (e) What is the coordination number for each ion? 10. The zinc blende lattice. The ZnS is zinc blende. The lattice consists of a fcc sulfide sub-lattice with Zn +2 cations occupying half (alternate) of the tetrahedral holes. (a) Sketch the ZnS lattice on this template. (b) What is the coordination number (number of nearest neighbors of opposite charge) for each ion? Day 10 Ionics 1 10

(c) How many S -2 anions are there per unit cell? Explain. 11. Diamond. Diamond has the same structure as zinc blende except that all of the occupied positions are taken by carbons (both the zinc cation and the sulfide anion positions. Sketch diamond here and connect every carbon to its four nearest neighbors. Do you see the tetrahedral angle? Review for the ACS Final Exam: Solid State 1. What is the empirical formula of a compound that crystallizes with anions in a fcc array sublattice with cations in half of the octahedral holes? A. MX B. MX 2 C. MX 4 D. M 2 X E. M 2 X 4 2. Calcium silicate crystallizes with oxygen ions in a fcc sublattice. The calcium ions occupy octahedral holes and the silicon atoms are in tetrahedral holes. What fraction of each type of hole is occupied? Octahedral Tetrahedral A. 1/4 1/8 B. 1/2 1/2 C. 1/4 1/2 D. 1/2 1/8 E. 1/8 1/4 3. Which of the following compounds would be most likely to exhibit the sodium chloride lattice? (a) MgO (b) K 2 S (c) CsCl (d) BeI 2 (e) RbI Answers: B, D, A Day 10 Ionics 1 11

Answers, Day 9. 1. Bronsted-Lowry concepts Summed: HNO 2 (aq) + H 2 O(aq) H 3 O + (aq) + NO - 2 (aq) K a = [H 3 O + ] x [NO - 2 ] / [HNO 2 ] NO - 2 (aq) + H 2 O(aq) OH - (aq) + HNO 2 (aq) K b = [OH - ] x [HNO 2 ] / [NO - 2 ] 2 H 2 O(aq) H 3 O + (aq) + OH - (aq) K = K a x K b = [H 3 O + ] x [OH - ] = K w (b) Complete this table of acid/base conjugate pairs. Acid K a Base K b chromic acid, H 2 CrO 4 1.8 x 10-1 HCrO - 4 5.6 x 10-14 hydrofluoric acid, HF 3.5 x 10-4 F - 2.9 x 10-11 phosphoric acid, H 3 PO 4 7.5 x 10-3 H 2 PO 4-1.3 x 10-12 dihydrogen phosphate, H 2 PO 4-6.2 x 10-8 HPO 4 2-1.6 x 10-7 hydrogen phosphate, HPO 4-2 4.8 x 10-13 PO 4 3-2.1 x 10-2 2. Lewis acid and base concepts Pb(OH)(OH 2 ) + 1.0 x 10-11 lead(ii) hydroxide, Pb(OH) 2 9.6 x 10-4 NH 4 + 5.6 x 10-10 ammonia, NH 3 1.8 x 10-5 CH 3 NH 3 + 2.7 x 10-11 methyl amine, CH 3 NH 2 3.7 x 10-4 Lewis acids: BF 3, Al +3, CPh 3 + (Ph = C 6 H 5 ), Fe +2, AlCl 3 ; Lewis bases: NH 3, H 2 O, F -, Cl - ; Neither: CH 4 3. Oxyacids Ranked strongest acid to weakest acid: HIO 4, HIO 3, HIO 2, HIO NaHSeO 4, NaHSeO 3, 4. Polyprotic acids K a = 10-12 - 10-13 for the second proton lost for germanic acid, and pk a = ~12 13 5. ph of salts LiCl, ph neutral; KBr, ph neutral; NH 4 NO 3, ph acidic; RbNO 2, ph basic; CsF, ph basic; Fe(ClO 4 ) 2, ph acidic; NaHSO 4, ph acidic; Na 2 SO 4, ph basic; NaC 2 H 3 O 2, ph basic 6. Hard-soft acid-bases chemistry. LiF + AgI LiI + AgF 2 KSCN + Hg(NO 3 ) 2 FeSCN + + PtCl 4-2 2 KNO 2 + Hg(SCN) 2 FeCl -2 4 + PtSCN + 7. Non-aqueous solvents. The 6 strong acids: HCl(aq), HBr(aq), HI(aq), HBO3(aq), HClO 4 (aq), H 2 SO 4 (aq) 2 H 2 O(aq) H 3 O + (aq) + OH - (aq) 2 HC 2 H 3 O 2 (aq) H 2 C 2 H 3 O + 2 (aq) + C 2 H 3 O - 2 (aq) 2 H 2 SO 4 (aq) H 3 SO 4 + (aq) + HSO 4 - (aq) The equilibrium that occurs when HCl and HBr are added to glacial acetic acid: HCl(aq) + HC 2 H 3 O 2 (aq) H 2 C 2 H 3 O + 2 (aq) + Cl - (aq) K = HBr(aq) + HC 2 H 3 O 2 (aq) H 2 C 2 H 3 O + 2 (aq) + Br - (aq) K = 8. Oxides. Na 2 O(s) + H 2 O(l) à 2 Na(OH)(aq) CaO(s) + H 2 O(l) à Ca(OH) 2 (s/aq) SO 3 (g) + H 2 O(l) à H 2 SO 4 (aq) SiO 2 + 2 OH - (aq) à SiO 2 (OH) 2-2 Amphoteric oxides. Some oxides are amphoteric. That is, they react with both acids and bases. Amphoteric oxides include BeO, Al 2 O 3, Ga 2 O 3, SnO 2, and PbO 2. Indicate them on the periodic table. Al 2 O 3, + 6 H 3 O + (aq) à 2 Al 3+ (aq) + 9 H 2 O(l) Al 2 O 3, + 2 OH - (aq) + 3 H 2 O(l) à 2 Al(OH) 4 - (aq) Day 10 Ionics 1 12