Chemistry 20 Lesson 11 Electronegativity, Polarity and Shapes

Similar documents
4 electron domains: 3 bonding and 1 non-bonding. 2 electron domains: 2 bonding and 0 non-bonding. 3 electron domains: 2 bonding and 1 non-bonding

Name: Period: Date: BONDING NOTES ADVANCED CHEMISTRY

ATOMIC ORBITAL MODEL OF THE ATOM Be able to draw rough sketches of s, p and d orbitals with different principal quantum numbers

Name: Period: Date: BONDING NOTES HONORS CHEMISTRY

Chapter 8 Predicting Molecular Geometries

Chem 115 POGIL Worksheet - Week 12 Molecular Shapes

Name Honors Chemistry / /

Midterm Review Notes - Unit 1 Intro

Name AP CHEM / / Chapter 8 Outline Bonding: General Concepts

Trimester 2 Exam 3 Study Guide Honors Chemistry. Honors Chemistry Exam 3 Review

SCIENCE 10: CHEMISTRY,

General Chemistry II, Unit II: Study Guide (part 1)

Interference is when two (or more) sets of waves meet and combine to produce a new pattern.

lecture 5: Nucleophilic Substitution Reactions

Principles of Organic Chemistry lecture 5, page 1

+ Charge attraction between a

Unit 9: The Mole- Guided Notes What is a Mole?

A Chemical Reaction occurs when the of a substance changes.

General Chemistry II, Unit I: Study Guide (part I)

Name: Period: Date: PERIODIC TABLE NOTES ADVANCED CHEMISTRY

Nuggets of Knowledge for Chapter 8 Chemical Reactions II Chem 2310

QCE Chemistry. Year 2015 Mark 0.00 Pages 20 Published Jan 31, Chemistry: Revision Notes. By Sophie (1 ATAR)

NOTES. Name: Date: Topic: Periodic Table & Atoms Notes. Period: Matter

Name: Period: Date: PERIODIC TABLE NOTES HONORS CHEMISTRY

Name: Period: Date: ATOMIC STRUCTURE NOTES ADVANCED CHEMISTRY

Unit 11 Solutions- Guided Notes. What are alloys? What is the difference between heterogeneous and homogeneous mixtures?

Semester 1 Honors Chemistry Notebook (unit 1)

CHAPTER Read Chapter 17, sections 1,2,3. End of Chapter problems: 25

Matter Content from State Frameworks and Other State Documents

Unit 14 Thermochemistry Notes

Chapter 9 Chemical Reactions NOTES

37 Maxwell s Equations

Nuggets of Knowledge for Chapter 10 Alkenes (I) Chem alkenes hydrocarbons containing a C=C (not in a benzene ring)

CHEM 1001 Problem Set #3: Entropy and Free Energy

Chem 116 POGIL Worksheet - Week 3 - Solutions Intermolecular Forces, Liquids, Solids, and Solutions

Flipping Physics Lecture Notes: Simple Harmonic Motion Introduction via a Horizontal Mass-Spring System

CRHS Academic Chemistry UNIT 5 - Periodic Table and Trends NOTES

State of matter characteristics solid Retains shape and volume

Types of Reactions 1. Acid-base: Transfer of protons, H+ 2. Substitution 3. Addition 4. Elimination 5. Oxidation and reduction: Loss and gain of O/H

making triangle (ie same reference angle) ). This is a standard form that will allow us all to have the X= y=

Course/ Subject: Chemistry I Grade: Teacher: Hill Oberto Month: September/October (6-8 weeks)

CHEM 103 Calorimetry and Hess s Law

LCAO APPROXIMATIONS OF ORGANIC Pi MO SYSTEMS The allyl system (cation, anion or radical).

Thermodynamics and Equilibrium

Acids and Bases Lesson 3

Name: Date: Class: a. How many barium ions are there per formula unit (compound)? b. How many nitride ions are there per formula unit (compound)?

Solutions to the Extra Problems for Chapter 14

, which yields. where z1. and z2

Chapter 15 Conjugated Systems

Building to Transformations on Coordinate Axis Grade 5: Geometry Graph points on the coordinate plane to solve real-world and mathematical problems.

1 The limitations of Hartree Fock approximation

CHEM 115 Course Review, Second Half

Sections 15.1 to 15.12, 16.1 and 16.2 of the textbook (Robbins-Miller) cover the materials required for this topic.

Thermodynamics Partial Outline of Topics

Fall 2013 Physics 172 Recitation 3 Momentum and Springs

In the spaces provided, explain the meanings of the following terms. You may use an equation or diagram where appropriate.

CHAPTER 24: INFERENCE IN REGRESSION. Chapter 24: Make inferences about the population from which the sample data came.

Flipping Physics Lecture Notes: Simple Harmonic Motion Introduction via a Horizontal Mass-Spring System

Lecture 5: Equilibrium and Oscillations

HW #2: 2.42, 2.44, 2.48, 2.50, 2.52, 2.58, 2.60, 2.62, 2.66, 2.68, 2.72, 2.82, 2.90, 2.96, 2.98

Differentiation Applications 1: Related Rates

PHYS 219 Spring semester Lecture 02: Coulomb s Law how point charges interact. Ron Reifenberger Birck Nanotechnology Center Purdue University

Chem 111 Summer 2013 Key III Whelan

Group Theory Problems

UNIT 12 Chemical Bonding

Lesson Plan. Recode: They will do a graphic organizer to sequence the steps of scientific method.

Guide to Using the Rubric to Score the Klf4 PREBUILD Model for Science Olympiad National Competitions

Modelling of Clock Behaviour. Don Percival. Applied Physics Laboratory University of Washington Seattle, Washington, USA

Plan o o. I(t) Divide problem into sub-problems Modify schematic and coordinate system (if needed) Write general equations

CHEM 116 Electrochemistry at Non-Standard Conditions, and Intro to Thermodynamics

O C S polar - greater force. H polar greater force. H polar. polar H-bond

NUMBERS, MATHEMATICS AND EQUATIONS

CHEM Thermodynamics. Change in Gibbs Free Energy, G. Review. Gibbs Free Energy, G. Review

CHAPTER 9 MODELS OF CHEMICAL BONDING

I. Analytical Potential and Field of a Uniform Rod. V E d. The definition of electric potential difference is

2004 AP CHEMISTRY FREE-RESPONSE QUESTIONS

20 Faraday s Law and Maxwell s Extension to Ampere s Law

SPH3U1 Lesson 06 Kinematics

Kepler's Laws of Planetary Motion

15.0 g Cr = 21.9 g Cr O g Cr 4 mol Cr mol Cr O

Trigonometric Ratios Unit 5 Tentative TEST date

CESAR Science Case The differential rotation of the Sun and its Chromosphere. Introduction. Material that is necessary during the laboratory

Bootstrap Method > # Purpose: understand how bootstrap method works > obs=c(11.96, 5.03, 67.40, 16.07, 31.50, 7.73, 11.10, 22.38) > n=length(obs) >

Lecture 17: Free Energy of Multi-phase Solutions at Equilibrium

AP Statistics Notes Unit Two: The Normal Distributions

Nuggets of Knowledge for Chapter 16 Ethers and Epoxides Chem 2320

UNIT 5: ATOMIC THEORY & THE PERIODIC TABLE CHEMISTRY 215, DUFFEY, CHAPTER 4 & SECTION 6.1

Experiment #3. Graphing with Excel

Introduction to Spacetime Geometry

Thermochemistry. Thermochemistry

ALE 21. Gibbs Free Energy. At what temperature does the spontaneity of a reaction change?

Physical Nature of the Covalent Bond Appendix H + H > H 2 ( ) ( )

Science 9 Unit 2: Atoms, Elements and Compounds

Chem 163 Section: Team Number: ALE 24. Voltaic Cells and Standard Cell Potentials. (Reference: 21.2 and 21.3 Silberberg 5 th edition)

Weathering. Title: Chemical and Mechanical Weathering. Grade Level: Subject/Content: Earth and Space Science

Five Whys How To Do It Better

Pipetting 101 Developed by BSU CityLab

A. Lattice Enthalpies Combining equations for the first ionization energy and first electron affinity:

CHAPTER 3 INEQUALITIES. Copyright -The Institute of Chartered Accountants of India

Chapters 29 and 35 Thermochemistry and Chemical Thermodynamics

Transcription:

Chemistry 20 Lessn 11 Electrnegativity, Plarity and Shapes In ur previus wrk we learned why atms frm cvalent bnds and hw t draw the resulting rganizatin f atms. In this lessn we will learn (a) hw the cmbinatin f bnded electrns and lne pairs f electrns result in different mlecular shapes and (b) hw unequal sharing f electrns within bnds alng with the shape f a mlecule result in plar and nnplar mlecules. I. Sterechemistry All mlecules have a definite three-dimensinal shape and the study f the shape f chemical cmpunds is called sterechemistry. T help us predict and understand the shapes f mlecules we use Valence-Shell-Electrn-Pair-Repulsin Thery (VSEPR Thery) which was develped by Rnald Nyhlm and Rn Gillespie in 1957. The name implies smething very ugly and cmplicated, but the thery is actually quite simple t understand and use. First f all, since electrns all have the same charge, they repel each ther. The VSEPR Thery prpses that valence electrn pairs, bth shared (bnding) and lne pairs, arrange themselves arund the central atm in a mlecule in such a way as t minimize repulsin between electrn pairs Thus, the bnding and lne pairs f electrns take-up psitins arund the central atm as far away frm ne anther as pssible. (Fr an alternate explanatin f sterechemistry refer t Nelsn Chemistry pages 91 t 103.) VSEPR thery results in five basic shapes that we will deal with: tetrahedral, pyramidal, angular, trignal planar, and linear. (Again, there are mre shapes that ccur in nature, but we will limit ur discussin t the five shapes that arise frm mlecules that frm based n the ctet rule.) Tetrahedral Fr mlecules like CH 4 r SiH 4 r CX 4 r SiX 4 (X represents a halgen) there are fur bnding pairs and zer lne pairs arund a central atm. The repulsin between the fur bnded pairs results is a tetrahedral shape. The shape is three-dimensinal. Therefre, in the shape diagram, dtted lines indicate that the bnd is directed int the plane f the paper and the wedge indicates the bnd is directed ut f the plane f the paper. The slid lines represent bnds that are in the plane f the paper. Dr. Rn Licht 11-1 www.structuredindependentlearning.cm

Trignal pyramidal Mlecules with three bnding pairs and ne lne pair arund a central atm assume a trignal pyramidal shape arund that central atm. Examples are: NH 3, PH 3, NX 3, PX 3. The pyramidal shape results frm the repulsin f the lne pair n the three bnding pairs. Angular Mlecules with tw bnding pairs and tw lne pairs arund a central atm assume an angular shape arund that central atm. Once again, the repulsin between lne pairs and bnded pairs causes the atms t have an angular shape. Examples include: H 2 O, H 2 S, OX 2, and SX 2 Trignal Planar The shape arund a central atm with three bnding pairs and zer lne pairs is trignal planar. T minimize repulsin, the three electrn pairs arund the central atm are directed t the crners f an equilateral triangle and the shape arund each carbn is described as being trignal planar. Tw imprtant ntes: 1) When deciding n the situatin arund a central atm, duble and triple bnds cunt as ne bnded pair. 2) It is very imprtant t understand that VSEPR thery predicts the shape arund a central atm nly. If there is mre than ne central atm in a mlecule, each central atm can have a different shape arund it. The mlecule mdel picture t the right shws tw central atms bnded tgether by a duble bnd with tw ther atms bnded t each central atm. VSEPR thery tells us that since each central atm has three bnded pairs (a duble bnd cunts as ne bnded pair) and n lne pairs, the shape arund each central atm is trignal planar central atm central atm Dr. Rn Licht 11-2 www.structuredindependentlearning.cm

Linear The shape arund atms with tw bnding pairs and zer lne pairs is linear. Examples include any carbn atm with a triple bnd in a hydrcarbn. In additin, diatmic mlecules (i.e. mlecules like H 2, O 2, HCl, etc.) are necessarily linear since there are nly tw atms invlved. Frm the descriptins f the shapes abve, we can see that if we knw the situatin f the electrn pairs surrunding a central atm we can predict the shape f the atms arund the central atm. The electrn pairs repel each ther and take up psitins as far frm ne anther as pssible. One may use the fllwing prcedure t predict the shape f a mlecule. 1. Draw the Lewis diagram r the structural diagram. 2. Cunt the number f lne pairs and bnding pairs arund the central atm. Remember that, fr the purpses f sterechemistry, single, duble and triple bnds all cunt as ne bnded pair. 3. Use the fllwing t find the shape: situatin arund central atm shape name diagram # LP # BP 0 4 tetrahedral 1 3 trignal pyramidal 2 2 angular 0 3 trignal planar 0 2 linear r Nw that we understand the shape f a mlecule we can start t understand hw different electrn distributins can lead t an imprtant phenmenn called plarity. But befre we can Dr. Rn Licht 11-3 www.structuredindependentlearning.cm

discuss this prperty in terms f sterechemistry, we must first discuss hw different electrn attracting abilities between atms results in altered electrn distributins. II. Electrnegativity In lessns 9 and 10 we learned abut the sharing f electrns t frm cvalent bnds. Hwever, experimental evidence indicates that cvalently bnded atms ften exhibit unequal attractins fr shared electrns. In ther wrds, when tw atms frm a bnd the shared electrns will spend mre time arund ne atm than the ther. In fact, different atms have different electrn attracting abilities. The relative attractin that an atm has fr shared electrns in a cvalent bnd is knwn as its electrnegativity. A scale f electrnegativities was develped by Linus Pauling fr which he wuld win the Nbel prize in 1954. The scale is a number in which the mst electrnegative atm, flurine, was assigned a value f 4.0. Examinatin f the electrnegativities f elements given in the peridic table indicates the fllwing trends. 1. Electrnegativities increase frm left t right within a perid. 2. Electrnegativities decrease frm tp t bttm within a grup. 3. Electrnegativities f the nn-metals are high while thse f the metals are lw. This bservatin is cnsistent with the fact that metals tend t lse electrns (lw electrnattracting-ability) and nn-metals gain electrns (high electrn-attracting-ability). Nte that the nly inert gas that has an electrnegativity value is xenn. This reflects the fact that inert elements nrmally d nt frm bnds. Hwever, sme clever chemists came up with a way t artificially induce xenn and flurine t frm xenn hexafluride. Further, electrn attracting ability is always t be understd in the cntext f a bnd r relatinship with ther atms. T speak f the electrnegativity f an individual atm des nt make sense. The electrnegativity scale is based n experimental evidence and reflects the relative reactivity f metals and nn-metals (i.e. the lwest electrnegativity belngs t the mst reactive metals, Cs and Fr, while the highest electrnegativity belngs t the mst reactive nn-metal, F). III. Plar and nn-plar cvalent bnds Hw des a difference in electrnegativity effect a cvalent bnd? The shared electrns within a bnd are mre strngly attracted t the atm with the higher electrn-attracting ability (i.e. higher electrnegativity). When we cmpare the electrnegativities fr hydrgen chlride, fr example, H Cl 2.2 3.2 the shared electrns will spend mre time arund Cl since it has a greater electrn attracting ability. In additin, since the bnding electrns (e ) are arund the Cl atm the majrity f the time, the Cl end f the mlecule becmes partially negative ( ) and the H end partially psitive (+). (+) H Cl ( ) Cvalent bnds in which the bnding electrns are unequally shared are called plar cvalent bnds. Plar cvalent bnds can be said t have a charge separatin r a bnd diple. Such a bnd diple can be represented by an arrw with the arrwhead pinting twards the partially Dr. Rn Licht 11-4 www.structuredindependentlearning.cm

negative, mre electrnegative, atm. If, n the ther hand, the atms invlved have the same electrn attracting ability the result is a nn-plar cvalent bnd. IV. Assignment part A In the fllwing diagrams draw an arrw t indicate the directin f the plar bnd. N H B F H C N I Br Cl C Cl N H C O H H F F I I S C Explain why cesium and francium are the mst reactive metals. Explain why flurine is the mst reactive nn-metal. V. Plarity f mlecules S far we have learned abut the sterechemistry f mlecules and plar/nn-plar cvalent bnds. In rder t determine the plarity f a mlecule, the sterechemistry f the mlecule must be knwn alng with the presence f bnd diples. The steps t be fllwed in determining the plarity f a mlecule are: 1. Draw a Lewis r structural diagram f the mlecule. When drawing a structural diagram remember that there may be lne pairs arund the central atm(s) that determine the shape f the mlecule. 2. Apply the VSEPR rules t draw r visualise the shape f the mlecule. In general, if a mlecule is trignal pyramidal r angular, the result is a plar mlecule. Fr the ther shapes cntinue t the next step. 3. Use electrnegativities t determine bnd diples and draw these n the shape/structural diagram. 4. Imagine the bnd diple arrws as frce vectrs. If bnd diples cancel r are symmetrical arund the central atms, the mlecule is nn-plar; if bnd diples d nt cancel, the mlecule is plar. In every case, bnd plarity is determined by additin f the bnd diples arrws in cncert with the directins they pint. Dr. Rn Licht 11-5 www.structuredindependentlearning.cm

The table belw summarises the situatins that give rise t mlecular plarity r nn-plarity when the atms bnded t the central atm are identical. If nn-identical atms are bnded t the central atm, the bnd diples may nt cancel. Fr example, CH 4 is nn-plar, but CH 3 Cl is plar because the C Cl bnd diple is nt cancelled by the C H bnd diples. Nte: It is very imprtant that yu, the student, d nt cnfuse a plar bnd with a plar mlecule. A plar bnd is the result f unequal sharing f electrns between tw atms within a mlecule. A plar mlecule is a mlecule that has an verall plarity due t the shape f the mlecule and/r the presence f bnd diples within the mlecule. Dr. Rn Licht 11-6 www.structuredindependentlearning.cm

VI. Assignment part B Fr each f the fllwing mlecules: a. draw the Lewis r structural diagram b. determine the shape arund the central atm(s) c. draw arrws t represent bnd diples d. determine whether the mlecule is plar r nt Mlecular Substance Lewis r structural diagram Shape Arund Central Atm(s) Shape Diagram & Bnd Diples Plarity f mlecule O O H 2 O angular plar H H H H HF NH 3 NH 4 + N 2 HBr OCl 2 C 2 H 2 SiCl 4 Dr. Rn Licht 11-7 www.structuredindependentlearning.cm

Mlecular Substance Lewis r structural diagram Shape Arund Central Atm(s) Shape Diagram & Bnd Diples Plarity f mlecule CO 2 CHI 3 C 2 H 3 Cl CH 4 C 2 H 6 C 2 H 4 CH 3 OH O 2 Dr. Rn Licht 11-8 www.structuredindependentlearning.cm

Mlecular Substance Lewis r structural diagram Shape Arund Central Atm(s) Shape Diagram & Bnd Diples Plarity f mlecule O 3 H 2 O 2 C 2 H 5 OH Dr. Rn Licht 11-9 www.structuredindependentlearning.cm