Adrian College : ELECTRONIC 607 : 13

Unformatted Document Excerpt

Coursehero >> Michigan >> Adrian College >> ELECTRONIC 607

Course Hero has millions of student submitted documents similar to the one
below including study guides, practice problems, reference materials, practice exams, textbook help and tutor support.

Course Hero has millions of student submitted documents similar to the one below including study guides, practice problems, reference materials, practice exams, textbook help and tutor support.

There is no excerpt for this document.

Find millions of documents on Course Hero - Study Guides, Lecture Notes, Reference Materials, Practice Exams and more. Course Hero has millions of course specific materials providing students with the best way to expand their education.

Below is a small sample set of documents:

Adrian College - ELECTRONIC - 607

1Basic Concepts1.11.21.31.41.51.6Systems of Units.Electric Charge.Current.Voltage.Power and Energy.Circuit Elements.DrDr Branislav HredzakAlexander and Sadiku, Fundamentals of Electric Circuits, Third Edition. McGraw-Hill2System of Units

body-comp-basics

Lone Star College System - ECON - 2301

When it comes to improving your physical appearance, your individual goals can bebroken down into two major categories. These are either getting leaner, or getting bigger.Getting a little bit bigger and a little bit leaner at the same time is generally

301 fall 2002 exam 2 key_1

VCU - CHEM - 301

Name_CHE 301: Organic Chemistry IFall, 2002Exam 21) Multiple choice. (45 pts)1) In a reaction energy diagram of a multistep reaction, which best describes the rate-determiningstep?a) the step that involves the highest energy transition stateb) the

All the R

VCU - CHEM - 301

FBrFBrAll the R/S designations will be changed in enantiomersIf there is a double bond, then its stereochemistry (cis/trans)will remain the same.BrBroA diastereomer is a non-superimposible non-mirror image.FBrFBrSome but not all of the R/S

Chapter 1

VCU - CHEM - 301

Chapter 5 StereochemistryChiralityo For a carbon to be chiral, it must have four different groups bondedto itMust be tetrahedral, but thats necessary for the above to betrue anyway.HHCCClBrCH3CH3chiralHBrachiralThus, CH3 or CH2 will neve

Chapter 4

VCU - CHEM - 301

Chapter 4HalogenationAddition of halogen to an alkaneoOnly works on sp3-hybridized carbonsWorks best with chlorine and bromineo Iodine is too slowo Fluorine blows up (too fast)Goes through radical intermediate, so putting halogen on more substitut

If the circle was clockwise

VCU - CHEM - 301

1H4Br23o If the circle was clockwise, then assign Ro If counterclockwise, then assign SWhat do I do if the #4 group is coming forward?Bro Still assign priorities to the different groups23Br41o Find R/S as though #4 was going back.23Br4

Meso compounds do not have to be cyclic

VCU - CHEM - 301

o Meso compounds do not have to be cyclicWhat is the relationship between these two compounds?ClClClClTheyre the same because if you rotate around the singlebonds you can get them into symmetrical forms.ClClClClTheyre two different drawings of

Chapter 5

VCU - CHEM - 301

Chapter 5 StereochemistryChiralityo For a carbon to be chiral, it must have four different groups bonded to itMust be tetrahedral, but thats necessary for the above to be trueanyway.HHCCClBrCH3CH3chiralHBrachiralThus, CH3 or CH2 will neve

Common question for this material

VCU - CHEM - 301

o Common question for this materialHow many monochorinated products, includingstereoisomers, will you get when you chlorinate a particularcompound.Ex.First, find all the positions that give you distinct structural isomers.Then, go through and see if

Enantiomers rotate light the same amount

VCU - CHEM - 301

Enantiomers rotate light the same amount, but inopposite directions.o So if one stereoisomer rotates light 4 to theright, then its enantiomer will rotate light 4 tothe left.o It is important to understand that R/Sconfiguration does not tell you whe

EXPT 6 resolution revised 101211

VCU - CHEM - 301

EXPT. 6: Resolution of a Racemic Mixture of Phenylsuccinic acidAs discussed in the polarimetry section of the techniques, enantiomers of a given compoundhave the same formula, but differ in the spatial arrangement of the atoms. The (+) isomer ofa set o

If you kept track of this as you did thi1

VCU - CHEM - 301

If you kept track of this as you did this, then you wouldhave something that looks like this:1,23,4,5,67,8,9,101112, 131415,16,17,1819,20ooIf you see, I just kept a tally of how many isomerswe had gotten to at each spot.So here, there are 2

If you kept track of this as you did this

VCU - CHEM - 301

Polarimetry

VCU - CHEM - 301

TECHNIQUE: PolarimetryWritten by Albert T. Sneden, VCU Department of Chemistry with revisions by L.M. MosesA large number of organic compounds, particularly those from natural sources, have a physicalproperty known as specific rotation which is reporte

Reflux

VCU - CHEM - 301

TECHNIQUE: Heating at RefluxWritten by Albert T. Sneden, VCU Department of Chemistry with revisions by L.M. MosesThere are many experiments in organic chemistry which call for heating the reactants in asolvent at the boiling point of the solvent for an

Chapter 2

VCU - CHEM - 102

Reactive Intermediates

VCU - CHEM - 102

Reactive IntermediatesCarbocationso Carbon with three bonds and no lone pairso Trigonal planar geometryosp2-hybridizedo empty p-orbitalo stability - 3>2>1> methylo electron-deficientoonly intermediate which can undergo rearrangementHhydride sh

The rest of chapter 4 that you should know from Gen Chem

VCU - CHEM - 102

The rest of chapter 4 that you should know from Gen ChemEquilibrium ConstantoKeq=oIf Keq> 1, then more products than reactantsoIf 0<Keq<1, then more reactants than productsoHe may ask you to propose a Keq for a reaction based on someinformation.

Columbia - IEOR - 4411

13

Document Preview

Unformatted Document Excerpt