SAN JOSE CITY COLLEGE INTRODUCTION TO CHEMISTRY 32B Spring February 18th, 2009 Chapters 29, 3,10-12 Bettelheim, 7 th ed.

Similar documents
SAN JOSE CITY COLLEGE INTRODUCTION TO CHEMISTRY 32B Spring March 9, 2009 Chapters 13, 14 and 17 Bettelheim, Brown, March

Chem 1120 Midterm points Dr. Luther Giddings

Chem 1220 Midterm points Dr. Luther Giddings

Moorpark College Chemistry 11 Fall Instructor: Professor Gopal. Examination #3: Section Three November 7, 2011.

CHEM 203 Exam 1. Name Multiple Choice Identify the letter of the choice that best completes the statement or answers the question.

Carbon Compounds. Chemical Bonding Part 2

Chapter 1 Reactions of Organic Compounds. Reactions Involving Hydrocarbons

12.1 The Nature of Organic molecules

Organic Chemistry is the chemistry of compounds containing.

CHEMISTRY 110 EXAM 2 Feb 25, 2013 FORM A

EXPERIMENT 1: Survival Organic Chemistry: Molecular Models

Chapter 12: Unsaturated Hydrocarbons

Chapter 25: The Chemistry of Life: Organic and Biological Chemistry

Chapter 12 Structure and Shape

Unit 5: Organic Chemistry

Introduction to Organic Chemistry. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Chapter 13 Alkenes and Alkynes Based on Material Prepared by Andrea D. Leonard University of Louisiana at Lafayette

Name: Class: Date: 3. How many lone pairs of electrons are assigned to the carbon atom in carbon monoxide? a. 0 b. 1 c. 2 d. 3

Chapter 4. An Introduction to Organic Compounds

Chem 1075 Chapter 19 Organic Chemistry Lecture Outline

Alkanes and Cycloalkanes

Time: 3 hours INSTRUCTIONS:

3. What number would be used to indicate the double bond position in the IUPAC name for CH 3 CH 2 CH=CH CH 3 a. 1 b. 2 c. 3 d.

CHEM Exam 1

Learning Organic Chemistry

Alkanes and Cycloalkanes

PSI Chemistry. 3) How many electron pairs does carbon share in order to complete its valence shell? A) 1 B) 2 C) 3 D) 4 E) 8

AP Chemistry Chapter 22 - Organic and Biological Molecules

Chemistry 201. MW 12pm 1:15pm Examination #1 July 20 th Bronco ID. Question Score Possible Points. 1 (17pts) 2 (28pts) 3 (14pts) 4...

Organic Chemistry. Unit 10

Unit 7 ~ Learning Guide Name:

EXPERIMENT 1: Survival Organic Chemistry: Molecular Models

Regents review Organic chemistry

Time Allowed: 60 minutes MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

CHE1502. Tutorial letter 203/1/2016. General Chemistry 1B. Semester 1. Department of Chemistry

Organic Chemistry. Organic chemistry is the chemistry of compounds containing carbon.

Chemistry 2.5 AS WORKBOOK. Working to Excellence Working to Excellence

Chemistry EXAM 1 (Fall Dr. Robertson)

Alkanes 3/27/17. Hydrocarbons: Compounds made of hydrogen and carbon only. Aliphatic (means fat ) - Open chain Aromatic - ring. Alkane Alkene Alkyne

Unsaturated hydrocarbons. Chapter 13

Chemistry 201. MW 12pm 1:15pm Examination #1 July 22 nd Bronco ID. Question Score Possible Points. 1 (10pts) 2 (24pts) 3 (14pts) 4...

3. Organic Compounds: Alkanes and Cycloalkanes

Chemistry 1A Spring 1998 Exam #4 KEY Chapters 9 & 10

Full file at

Chapter 22. Organic and Biological Molecules

Organic Chemistry. Alkenes (2)

MOLECULAR REPRESENTATIONS AND INFRARED SPECTROSCOPY

MOSTLY ALCOHOLS. Question 2, 2017 The structure of a molecule of an organic compound, threonine, is shown below.

DO NOT OPEN THE EXAMINATION PAPER UNTIL YOU ARE TOLD BY THE SUPERVISOR TO BEGIN CHEMISTRY 2202 SAMPLE EXAMINATION. June, 2008

Chem 121 Winter 2016: Section 03, Sample Problems. Alkenes and Alkynes

Name: Unit 11 Organic Chemistry

INTRODUCTION TO ORGANIC CHEMISTRY: ALKANES

Common Elements in Organic Compounds

Unit 2 Review: Organic Chemistry. 1. Terms for which you should be able to write or apply the definitions:

Level 2 Chemistry, 2013

Classes of Organic Compounds

STRUCTURE, ISOMERISM AND NOMENCLATURE OF ORGANIC COMPOUNDS

EXPERIMENT 8 Reactions of Hydrocarbons

Organic Chemistry SL IB CHEMISTRY SL

Isomerism in Alkanes, Haloalkanes, and Alkenes using Molecular Models

Name Chemistry 10 Dr. Kline 11 May 2004 Row Seat Lab 8:00 10:30

Organic and Biochemical Molecules. 1. Compounds composed of carbon and hydrogen are called hydrocarbons.

St. Charles College Final Exam 12U Chemistry Teacher: Mrs. D. Johnston Time: 2 hours Marks: 108

1.8. Organic Chemistry. Practice Exam Organic Chem. System LENGTH: VOLUME MASS Temperature. 1 gal = 4 qt. 1 lb = 16 oz.

Chapter 13 Alkenes and Alkynes & Aromatic Compounds

Chemistry 11 Hydrocarbon Alkane Notes. In this unit, we will be primarily focusing on the chemistry of carbon compounds, also known as.

CH320/328 M Spring 2014

Organic Chemistry Worksheets

75. A This is a Markovnikov addition reaction. In these reactions, the pielectrons in the alkene act as a nucleophile. The strongest electrophile will

A. They all have a benzene ring structure in the molecule. B. They all have the same molecular formula. C. They all have carbon and hydrogen only

Name: Teacher: DO NOT OPEN THE EXAMINATION PAPER UNTIL YOU ARE TOLD BY THE SUPERVISOR TO BEGIN. Chemistry FINAL EXAMINATION June 2010

CHAPTER 2: Structure and Properties of Organic Molecules

Lewis Structures. Lewis Structures. Lewis Structures. Lewis Structures. What pattern do you see? What pattern do you see?

PART 3 Chemical Bonds, Valence Bond Method, and Molecular Shapes. Reference: Chapter 9 10 in textbook

Chemistry /002 Exam 1 Version Green. The Periodic Table

8. What is the slow, rate-determining step, in the acidcatalyzed dehydration of 2-methyl-2-propanol?

The Final Learning Experience

4. Based on the following thermochemical equation below, which statement is false? 2 NH 3 (g) N 2 (g) + 3 H 2 (g) H = kj

Reactions of Chapter 10 Worksheet and Key

MSC. ISMAIL M.ALI DEPARTMENT OF CHEMICAL ENGINEEING COLLEGE OF ENGINEERING TIKRIT UNIVERSITY

CHEM 203. Midterm Exam 1 October 31, 2008 ANSWERS. This a closed-notes, closed-book exam. You may use your set of molecular models

Level 2 Chemistry, 2017

Hour Examination # 1

Practice Packet Unit 11: Organic Chemistry

HYDROCARBONS. Section A

Chapter 8 Alkenes and Alkynes II: Addition Reactions. Alkenes are electron rich. Additions to Alkenes

CHAPTER 2. Structure and Reactivity: Acids and Bases, Polar and Nonpolar Molecules

Please read and sign the Honor Code statement below:

Assessment Schedule 2016 Chemistry: Demonstrate understanding of the properties of selected organic compounds (91165)

9. Which compound is an alcohol? A) methanol C) butane B) ethyne D) propanal

1. Which is the most electronegative atom in the compound below?

Part I. Multiple choice. Circle the correct answer for each problem. 3 points each

CHEMISTRY 2202 FINAL EXAMINATION Value: 100% General Instructions

Chapter 3. Organic Compounds: Alkanes and Their Stereochemistry

Chapter 8 Chemical Bonding

Ch08. Carbonyls. The carbonyl functional group. Exploring ketones, aldehydes and their reactions. version 1.0

Unit 14: Organic Chemistry REGENTS CHEMISTRY

Chemistry 110. Bettelheim, Brown, Campbell & Farrell. Introduction to General, Organic and Biochemistry Chapter 12 Alkenes & Alkynes.

Chemistry 110 Bettelheim, Brown, Campbell & Farrell Ninth Edition Introduction to General, Organic and Biochemistry Chapter 12 Alkenes & Alkynes

I. Multiple Choice Questions (Type-I)

Transcription:

SAN JOSE CITY COLLEGE INTRODUCTION TO CHEMISTRY 32B Spring 2009 Name: ID#: Instructor: Dr. Tyler Johnson Time Allowed:1h 20 min February 18th, 2009 Chapters 29, 3,10-12 Bettelheim, 7 th ed 100 Points LEARNING FESTIVILE (I) I hereby affirm that I will abide by the Academic Integrity Code of San Jose City College. That is, I will not cheat on this exam. Your Signature: Instructions: The exam consists of 20 multiple choice (3 points each) and 9 short answer questions (40 points). Indicate your answers to the multiple choice questions by writing the letter choice in the space provided in the answer sheet, below. Write your short answers in the space provided. A periodic table is attached at the end of the exam. The periodic table can be detached. Answer ALL the questions. Make efficient use of your time. Do the problems which are easy first, and leave the more difficult ones to last. Don t spend too much time on any one problem. Remember to use significant figures when reporting numerical answers. Note: Partial credit is given where possible if, and only if, you support your answer by detailing your work, including possible/partial structures and/or providing your reasoning. SHOW YOUR WORK! Select the BEST answer to the multiple choice questions below. Indicate your answers to the multiple choice questions by writing the letter choice on a scantron (You may also place the answer in the space provided in the answer sheet, below, but this will not be graded). (3 pts ea): 1 b. 2 a. 3 a. 4 d. 5 a. 6 b. 7 e. 8 e. 9 b. 10 a. 11 a. 12 c 13 d 14_c 15 a 16 d 17 b 18 c_ 19_d 20 a 1

MULTIPLE CHOICE QUESTIONS (60 POINTS) (((ANSWERS ON PAGE 1)) 1. For the structure shown, the most likely elements are X = and Y =..... :Y = X = Y: a. oxygen, nitrogen b. carbon, oxygen c. carbon, hydrogen d. oxygen, carbon e. oxygen, hydrogen 2. A chemical bond formed when two atoms share six electrons is a bond; it is best described as. a. triple; covalent b. single; covalent c. double; ionic d. double; covalent e. triple; ionic 3. Identify the boxed functional group below a. primary amine b. secondary amine c. tertiary amine d. primary alcohol e. carboxylic acid 4. Which element is likely to form two covalent bonds? a. C b. Si c. N d. O e. Se 5. In organic chemistry, the term saturated means a molecule a. Which has the maximum number of carbon-hydrogen bonds possible. b. With a specific six-membered ring structure. c. Which contains one or more multiple bonds between carbon atoms. d. Which can react by taking up one or more water molecules. e. Which is formed from many smaller molecules. 6. The cause of cis-trans isomerism is a. Stability of the double bond. b. Lack of rotation of the double bond. c. Strength of the double bond. d. Short length of the double bond. e. Vibration of the double bond. 2

7. Identify the boxed functional groups a. a primary alcohol and carboxylic acid b. a secondary alcohol and carboxylic acid c. a tertiary alcohol and carboxylic acid d. a primary alcohol and aldehyde e. a secondary alcohol and aldehyde 8. A molecule in which the central atom forms two single and 1 double bond and has no lone pair is said to have a shape. a. bent b. linear c. tetrahedral d. pyramidal e. trigonal planar 9. What is the IUPAC name of the following compound? a. 1,5 dimethylhexane. b. 2,5 dimethylhexane c. 2,2 dimethylhexane d. 2,5,5 trimethylpentane e. 2,2,5 trimethylpentane 10. Are the following molecules constitutional isomers? a. yes b. no 11. When an alkene undergoes a hydrogenation reaction the product is an a. alkane b. alkyne c. alkene d. alcohol e. ether 12. What is the IUPAC name of the following molecule: CH 2 =CH-CH 2 -CH=CH-CH 3 a. 1,2-hexadiene b. 1,3-hexadiene c. 1,4-hexadiene d. 2,5-hexadiene e. 3,6-hexadiene 3

13. Which molecule can have cis-trans isomers? a. CH 3 CH=C(CH 3 ) 2 b. (CH 3 ) 2C=CHCH 3 c. (CH 3 ) 2C=C(CH 3 ) 2 d. CH 3 CH=CHCl e. CH 3 CH=CCl 2 14. Which of the following reagents is necessary to complete the following RXN: a. H 2 O (H 2 SO 4 ) b. H 2 (Pd) c. HBr d. Br 2 e. KMnO 4 15. When an alkene undergoes hydration, the product is a(n) a. alcohol b. aromatic c. alkane d. alkyl halide e. alkyne 16. In converting 1-butene, which of the following reagents does NOT exhibit Markovnikov's rules of addition? a. H 2,(Pd) b. H 2 O (H 2 SO 4 ) c. Br 2 d. a and c e. None of the above. 17. How many carbon-carbon double bonds in lycopene (see below) have the possibility for cis/trans isomerism? a. 2 10 b. 2 11 c. 2 12 d. 2 13 e. None of the above. 4

18. The average non exercising human requires approximately how many calories per day to maintain normal metabolism? (i.e neither gain nor loose weight) a. 1000 b. 1500 c. 2000 d. 3000 e. 5000 19. The vegetarian presents with anemia and fatigue. The nurse suspects that the vegetarian is deficient in a. Vitamin C b. Vitamin D c. Vitamin B2 (or thiamine) d. Folic acid e. Magnesium 20. Which dietary source of energy yields approximately 9kcal/gram? a. fat b. protein c. fiber d. carbohydrate e. grain SHORT ANSWER QUESTIONS (40 points) 1. Draw the mechanism for the reaction of HBr reacting with the molecule shown. Include intermediates. Draw the structure of the product(s). If there is more than one product, label the minor and major product. Briefly explain the guiding principle or rule that this reaction demonstrates. [6 pts] (CH 3 ) 2C=CHCH 2 CH 3 + HBr see practise exam KEY same problem 5

2. Draw a structural formula for the one tertiary (3 ) alcohol with a molec. formula C 4 H 10 O (2 pts.) (CH3) 3 CHOH 3. For the following reactions, predict the starting material, reagent(s), and/or major product(s). [8 pts, 2 pts each]. In all cases, assume that you have excess of the reagent. You do not need to draw a mechanism. (a) Structure + HI 2-Ido-octane CH2=CH-(CH2) 5 CH3 OH (b) CH 3 CH=CH 2 + H 2 O/ /H 2 SO 4 (hydration) CH 3 CH-CH 3 (c) + Br 2 (Bromination) 1,2, di-bromocyclohexane (CH 2Cl 2) (d) CH 2 =CHCH 2 CH 3 + H 2 /catalyst (hydrogenation/reduction) CH 3 -CH 2 -CH 2 CH 3 4. Clearly draw the cis isomer for: (4 pts.) (a) CH 2 =CH-CH=CHCH 3 (b) 1,2-dimethylcyclohexane CH 3 ch 3 OR OR 5. The correct formula for formaldehyde, is CH 2 O. Electronegativity values are C= 2.5, H =2.1, O =3.5 (a) Draw the Lewis dot structure for formaldehyde (a common preservative) O (b) Is the molecule polar covalent, nonpolar covalent or ionic? (c) What is the shape of the molecule, tetrahedral, trigonal planar, pyramidal or linear? 6 H H

(d) Give the predicted bond angles. 109.5, 120, 180 [8 pts] 6. What is the IUPAC name for the compound below: [3 pts] Cl CH 3 CH 2 CH 3 CH 3 CH CH 2 - C CH 2 CH CH 2 CH CH 3 CH 3 CH 2 CH 3 2-chloro,6ethyl, 4,4,8 trimethyldecane 7. Using the line- or angle-bond representations, draw the structure of 4-ethyl- 2,2,di-methylhexane [3 pts] 8. The reaction of Chlorine (Cl 2 ) with pentane (under UV light or Heat) gives a mixture of three chloroalkanes with a molecular formula of C 5 H 11 Cl. Write the line angle formula for each [3 pts] see HW 11.46 9. One reaction that we conducted in lab was to add KMnO4 to cyclohexene in a test tube. Draw the structure of the product(s) when these two substances are mixed. Would this reaction give a positive or negative (circle one) test result. Please explain and predict what you would expect to observe. [3 pts] See practice exam Key, same Q. Extra Credit. Draw all the isomers of C 2 Br 2 H 2. [6 pts] Br Br Br Br Br Br 7

Note: Ia = 1 IIa = 2 IIIa = 3 IVa = 4 Va = 5 VIa = 6 VIIa = 7 8