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Lehigh University School Information

School Facts

  • Operating Status: Currently operating

    Campus: Main campus (and distance learning)

    Institution Type: 3

  • Degree Type:

    Distance Education: On-campus and Online

Admissions

33%

32%

Admission Selectivity and Test Scores
SAT

72%

Average SAT Score Range

  • Unknown

ACT

28%

Average ACT Score

  • Unknown

Info IconAt Lehigh University, 72% of students submitted the SAT score, but Lehigh University accepts both SAT and ACT.

Admission Requirement
AP Credits
Yes

Academics

Graduation Rate

  • 78%

  • 88%

  • 89%

Degree Details

Available Fields of Study and Degrees

  • > Accounting Bachelor's Program, Master's Program
  • > African Studies Bachelor's Program
  • > American/United States Studies/Civilization Bachelor's Program, Master's Program
  • > Ancient Studies/Civilization Bachelor's Program
  • > Anthropology Bachelor's Program
  • > Applied Mathematics, General Master's Program
  • > Architectural History and Criticism, General Bachelor's Program
  • > Architecture Bachelor's Program
  • > Art History, Criticism and Conservation Bachelor's Program
  • > Art/Art Studies, General Bachelor's Program
  • > Asian Studies/Civilization Bachelor's Program
  • > Astronomy Bachelor's Program
  • > Astrophysics Bachelor's Program
  • > Biochemistry Bachelor's Program
  • > Bioengineering and Biomedical Engineering Bachelor's Program, Master's Program
  • > Biological and Physical Sciences Bachelor's Program
  • > Biology/Biological Sciences, General Bachelor's Program, Master's Program
  • > Business Administration and Management, General Master's Program
  • > Business/Managerial Economics Bachelor's Program, Master's Program
  • > Chemical and Biomolecular Engineering Master's Program
  • > Chemical Engineering Bachelor's Program, Master's Program
  • > Chemistry, General Bachelor's Program, Master's Program
  • > Chinese Language and Literature Bachelor's Program
  • > Civil Engineering, General Bachelor's Program, Master's Program
  • > Classics and Classical Languages, Literatures, and Linguistics, General Bachelor's Program
  • > Cognitive Science Bachelor's Program
  • > Computer and Information Sciences and Support Services, Other Bachelor's Program
  • > Computer Engineering, General Bachelor's Program, Master's Program
  • > Computer Science Bachelor's Program, Master's Program
  • > Counseling Psychology
  • > Counselor Education/School Counseling and Guidance Services Master's Program
  • > Curriculum and Instruction
  • > Design and Visual Communications, General Bachelor's Program
  • > Drama and Dramatics/Theatre Arts, General Bachelor's Program
  • > Education, Other Master's Program
  • > Educational Leadership and Administration, General Master's Program
  • > Educational/Instructional Technology Master's Program
  • > Electrical and Electronics Engineering Bachelor's Program, Master's Program
  • > Elementary Education and Teaching Master's Program
  • > Engineering Physics/Applied Physics Bachelor's Program
  • > Engineering, Other Bachelor's Program, Master's Program
  • > English Language and Literature, General Bachelor's Program, Master's Program
  • > Entrepreneurial and Small Business Operations, Other Master's Program
  • > Environmental Studies Bachelor's Program
  • > Environmental/Environmental Health Engineering Bachelor's Program, Master's Program
  • > Evolutionary Biology Master's Program
  • > Finance, General Bachelor's Program, Master's Program
  • > French Language and Literature Bachelor's Program
  • > Geological and Earth Sciences/Geosciences, Other Bachelor's Program, Master's Program
  • > Geology/Earth Science, General Bachelor's Program, Master's Program
  • > German Language and Literature Bachelor's Program
  • > History, General Bachelor's Program, Master's Program
  • > Industrial Engineering Bachelor's Program, Master's Program
  • > Information Science/Studies Bachelor's Program, Master's Program
  • > International and Comparative Education Master's Program
  • > International Business/Trade/Commerce Master's Program
  • > International Relations and Affairs Bachelor's Program
  • > International/Global Studies Bachelor's Program
  • > Journalism Bachelor's Program
  • > Logistics, Materials, and Supply Chain Management Bachelor's Program, Master's Program
  • > Management Information Systems and Services, Other Master's Program
  • > Management Information Systems, General Bachelor's Program
  • > Management Science Bachelor's Program, Master's Program
  • > Manufacturing Engineering Master's Program
  • > Marketing/Marketing Management, General Bachelor's Program, Master's Program
  • > Materials Engineering Bachelor's Program, Master's Program
  • > Mathematics, General Bachelor's Program, Master's Program
  • > Mechanical Engineering Bachelor's Program, Master's Program
  • > Molecular Biology Bachelor's Program, Master's Program
  • > Multi-/Interdisciplinary Studies, Other Bachelor's Program
  • > Music History, Literature, and Theory Bachelor's Program
  • > Music, General Bachelor's Program
  • > Natural Resources Management and Policy Master's Program
  • > Neuroscience Bachelor's Program, Master's Program
  • > Philosophy Bachelor's Program
  • > Physics, General Bachelor's Program, Master's Program
  • > Political Science and Government, General Bachelor's Program, Master's Program
  • > Polymer/Plastics Engineering Master's Program
  • > Pre-Dentistry Studies Bachelor's Program
  • > Pre-Medicine/Pre-Medical Studies Bachelor's Program
  • > Project Management Master's Program
  • > Psychology, General Bachelor's Program, Master's Program
  • > Religion/Religious Studies Bachelor's Program
  • > Russian Studies Bachelor's Program
  • > School Psychology Master's Program
  • > Science, Technology and Society Bachelor's Program
  • > Secondary Education and Teaching Master's Program
  • > Social and Philosophical Foundations of Education
  • > Sociology Bachelor's Program, Master's Program
  • > Spanish Language and Literature Bachelor's Program
  • > Special Education and Teaching, General Master's Program
  • > Statistics, General Bachelor's Program, Master's Program
  • > Structural Engineering Bachelor's Program, Master's Program
  • > Student Counseling and Personnel Services, Other Master's Program
  • > Systems Engineering Master's Program
  • > Technical and Scientific Communication Bachelor's Program
  • > Urban Studies/Affairs Bachelor's Program
  • > Women's Studies Bachelor's Program

Tuition, Cost and Financial Aid

  • Undergraduate Tuition

    • In-State Tuition (2014-2015)

      $44,520.00

    • Out-of-State Tuition (2014-2015)

      $44,520.00

Financial Aid — Freshmen Students
Type of Aid No. Receiving Aid % Receiving Aid Total Aid Received Average Aid Received
Any Student Financial Aid 793 66% - $4,326.00
Grant Aid 595 50% $17,351,028.00 $27,608.00
Student Loan - 46% - $4,419.00
Financial Aid — Undergraduate Students
Type of Aid No. Receiving Aid % Receiving Aid Total Aid Received Average Aid Received
Any Student Financial Aid 2,537 51% $75,047,771.00 $29,581.00
Pell Grant Aid 728 15% $3,121,987.00 $4,288.00
Student Loan 2,168 44% $13,774,317.00 $6,353.00

Students

Student-Faculty Ratio

10 : 1

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Endowment per FTE Enrollment

$182,654

per student

Demographics

Source: National Center for Education Statistics (NCES), Institute of Education Sciences, 2014 - 2015

Course Hero, Inc. does not independently verify the accuracy of the information presented above.

Lehigh University Documents (18,763)

Master your classes with homework help, exam study guides, past papers, and more for LU.

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  • 17 pages Marketing 111 Study Guide ch. 8-xx.docx
    • Marketing 111 Study Guide ch. 8-xx.docx
    • Lehigh University
    • Introduction to Marketing
    • MARKETING 001 - Fall 2016
    • Marketing 111 Study Guide (ch. 8-14) Chapter 8: New product development and product life cycle strategies New product development strategy and process: = New product development: development of new products, improvements, and new brands by a firm 1) Id
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    Marketing 111 Study Guide ch. 8-xx.docx

  • 14 pages Marketing 111 Study Guide ch. 1-7.docx
    • Marketing 111 Study Guide ch. 1-7.docx
    • Lehigh University
    • Introduction to Marketing
    • MARKETING 001 - Fall 2016
    • Marketing 111 Study Guide (ch. 1-7) Chapter 1: What is marketing? Managing profitable customer relationships Marketing defined: Satisfying customer needs Marketing mix: A set of marketing tools that work together to satisfy customer needs and build custo
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    Marketing 111 Study Guide ch. 1-7.docx

  • 1 pages Chad Notes.46.pdf
    • Chad Notes.46.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Friedel-Crafts Alkylation R-X/AlCl3 -Fails with strongly deactivated benzenes (benzenes with strong electron withdrawing groups attached) -will still work with a halogenated benzene but not with anything less reactive than this -Carbocation rearrangements
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    Chad Notes.46.pdf

  • 1 pages Chad Notes.60.pdf
    • Chad Notes.60.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • O O Michael Addition (also called -addition or conjugate addition) O O EtO OEt OEt O EtO O O Michael Addition with a lithium dialkylcuprate (Gilman reagent) (CH3)2CuLi H2O Wittig Rxn Addition of a phosphylide to form an alkene R1 R1 O CH3 R2 PPh3 R2 R1 Fo
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    Chad Notes.60.pdf

  • 1 pages Chad Notes.63.pdf
    • Chad Notes.63.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Fischer Esterification O + HO R OH O + H R O + H O H Saponification O OH O O R1 O O O R2 - XS OH OH + O O R1 OH glycerol R3 + O O R2 + O O R3 f atty acid carboxylates Gabriel Synthesis O O O . 1 KOH NH . 2 R Br Ba(OH)2 N R O O R or NH2NH2 NH2 O + O O Conv
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    Chad Notes.63.pdf

  • 1 pages Chad Notes.67.pdf
    • Chad Notes.67.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Aldol Condensation Acid catalyzed - enol adds to a ketone or aldehyde Base-catalyzed - enolate adds to a ketone or aldehyde O O 2 O - OH or acid HO a -ketoalcohol heat a conjugated enone 66
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    Chad Notes.67.pdf

  • 1 pages Chad Notes.73.pdf
    • Chad Notes.73.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Reduction of Amides (1. LiAlH4 2. H3O+ ) . O 1 LiAlH 4 NH2 . + 2 H3O NH2 Hofmann Rearrangement O NaOBr or NH2 Br2, OH NH2 Curtius R CO2H Schmidt 1. SOCl2 2. NaN3 R NH2 R CO2H 3. heat / H2O Beckman Rearrangement O NOH NH2OH + H NaN3 / H2SO4 R NH2 O PCl5 NH
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    Chad Notes.73.pdf

  • 1 pages Chad Notes.55.pdf
    • Chad Notes.55.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • DIBALH reduces esters to aldehydes . O 1 DIBALH 78oC O . 2 H2O O H Lithium tri-t-butoxy aluminum hydride reduces acid chlorides to aldehydes O O LiAl[OC(CH3)3]3H - o 78 C Cl H H2, Pd/C reduces alkenes, alkynes, and nitro groups OH O H 2 Pd/C O H2 H OH Pd/
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    Chad Notes.55.pdf

  • 1 pages Chad Notes.27.pdf
    • Chad Notes.27.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Free Radical Halogenation Reactions Summary Free Radical Bromination (high selectivity) Free Radical Chlorination (low selectivity) Allylic/Benzylic Bromination Br2 Br light or heat Cl2 Cl light or heat NBS Cl + Br light or heat or peroxide NBS Br light o
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    Chad Notes.27.pdf

  • 1 pages Chad Notes.62.pdf
    • Chad Notes.62.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Nucleophilic Acyl Substitution -Reactivity (acid chlorides > anhydrides > esters > amides > carboxylates) O SOCl2 (or PBr3 f or acid bromides) R Cl acid chloride O O O R or OH O R R O acid anhydride R O + R'OH / H O HO R carboxylic acid 3O + /D O 2eq R2NH
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    Chad Notes.62.pdf

  • 1 pages Chad Notes.45.pdf
    • Chad Notes.45.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Electrophilic Aromatic Substitution E H E E E E H H B EAS Reaction / Reagents Electrophile NO2 HNO3 NO2 Name Nitration H2SO4 SO3H SO3 SO3H H2SO4 SO3H H SO 2 4 n/a Cl Cl2 Sulfonation Desulfonation or Cl Cl Cl AlCl3 Chlorination AlCl3 Br Br2 Br FeBr3 Br FeB
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    Chad Notes.45.pdf

  • 1 pages Chad Notes.43.pdf
    • Chad Notes.43.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Alcohol Reactions Summary I Conversion to an alkyl iodide OH HI Conversion to an alkyl bromide OH HBr Conversion to an alkyl chloride OH HCl ZnCl Conversion to an alkyl chloride with thionyl chloride (only for 1 and 2) Conversion to an alkyl bromide (only
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    Chad Notes.43.pdf

  • 1 pages Chad Notes.24.pdf
    • Chad Notes.24.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 12 Radical Reactions Chlorination vs Bromination 1) Cl2 / h (not very selective) 2) Br2 / h (highly selective) Selectivity and stability of radicals (chlorination vs. bromination) Mechanism h Cl Cl + CH 4 Ea = 17kJ CH3 + Cl 2Cl Ho = 243kJ 2Cl Cl C
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    Chad Notes.24.pdf

  • 1 pages Chad Notes.44.pdf
    • Chad Notes.44.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 17 Aromatic Compounds Nomenclature O O benzoic acid benzaldehyde anisole phenol NH2 aniline OCH3 OH H OH CH3 CH3 styrene toluene o-xylene CH3 Criteria for Aromatic Compounds 1) Cyclic and conjugated 2) Each atom in the ring must have an unhybridiz
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    Chad Notes.44.pdf

  • 1 pages Chad Notes.51.pdf
    • Chad Notes.51.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 18 Ketones and Aldehydes Nomenclature aldehydes as the main functional group: -al ending aldehydes as a substituent: formyl (or oxo) ketones as the main functional group: -one ending ketones as a substituent: oxo Synthesis Oxidation using chromic
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    Chad Notes.51.pdf

  • 1 pages Chad Notes.39.pdf
    • Chad Notes.39.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 16 Alcohols, Ethers, and Epoxides Alcohols Nomenclature As the main functional group: -ol ending As a substituent: hydroxy Acidity of Alcohols General trend: Methyl > 1 > 2 > 3 OH H3C pK OH a~ . 15 5 OH pK a~ pKa 16 ~ OH 17 pKa ~ 19 Acidity of Phe
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    Chad Notes.39.pdf

  • 1 pages Chad Notes.41.pdf
    • Chad Notes.41.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Oxidation of Alcohols Na2Cr2O7/H2SO4 oxidizes 1 alcohols to carboxylic acids, 2 alcohols to ketones, and aldehydes to acids O OH Na2Cr2O7 OH Na2Cr2O7 OH H2SO4 H2SO4 O H O Na2Cr2O7 H2SO4 OH O PCC oxidizes 1 alcohols to aldehydes and 2 alcohols to ketones H
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    Chad Notes.41.pdf

  • 1 pages Chad Notes.34.pdf

    Chad Notes.34.pdf

  • 1 pages Chad Notes.31.pdf

    Chad Notes.31.pdf

  • 1 pages Chad Notes.77.pdf
    • Chad Notes.77.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 22 Carbon-Carbon Coupling Reactions Gilman Reagent (lithium dialkyl cuprate with conjugated carbonyl) Heck (vinyl halide with conjugated ester, nitrile, or aldehyde with Pd(PAr3)4 and Et3N ) O O I + Pd[(Ar3)]4 OCH3 (Et)3N Suzuki OCH3 B OCH3 H3CO B
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    Chad Notes.77.pdf

  • 1 pages Chad Notes.54.pdf
    • Chad Notes.54.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Hydride Reduction Reactions NaBH4 reduces ketones, aldehydes, and acid halides OH O NaBH O 4 EtOH . 1 NaBH4 O Cl NaBH4 H . + 2 H3O OH EtOH OH LiAlH4 reduces ketones, aldehydes, acid chlorides, esters, carboxylic acids, and amides (and others) . OH . O OH
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    Chad Notes.54.pdf

  • 1 pages Chad Notes.21.pdf
    • Chad Notes.21.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 11 Elimination Reactions E2 reactions Elimination Bimolecular H3C CH3 B H X H H rate = k[substrate][base] H and X (leaving group) should be anti-periplanar (anti-coplanar) Typically forms most substituted double bond (Zaitsevs Rule) Forms least su
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    Chad Notes.21.pdf

  • 1 pages Chad Notes.50.pdf
    • Chad Notes.50.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Nucleophilic Aromatic Substitution (NAS) strong nucleophile (NH2- or OH- for example) replaces halide electron withdrawing groups ortho/para to halide facilitate reaction 1) Addition-Elimination Mechanism Cl NH2 Cl NO2 NO2 Na NH2 NO2 NH2 NO2 NO2 NO2 2) Be
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    Chad Notes.50.pdf

  • 1 pages Chad Notes.48.pdf
    • Chad Notes.48.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Side-Chain Reactions of Benzenes Permanganate Oxidation O . 1 KMnO4, OH , boil . 2 H3O+ Chromic acid (Na2Cr2O7 / H2SO4) achieves the same result OH HO O Side-chain Reduction Clemmenson Reduction reduces ketones and aldehydes to alkanes O Zn (Hg) Wolff Kis
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    Chad Notes.48.pdf

  • 1 pages Chad Notes.33.pdf
    • Chad Notes.33.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Chapter 15 NMR Spectroscopy 13 C NMR Gives the number of carbon environments in a molecule The chemical shift also tells whether the carbon is an alkane, alkene, aromatic, or carbonyl (C=O) 1 H NMR -Gives the number of hydrogen environments in a molecule
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    Chad Notes.33.pdf

  • 1 pages Chad Notes.57.pdf
    • Chad Notes.57.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Addition to a Conjugated Carbonyl NaBH4/CeCl3 and organolithium add to the carbonyl (1,2-addition) Grignards often result in both 1,2- and 1,4-addition CN-, OH-, R2CuLi, and bulky grignards add to the carbon (1,4-addition) O O (CH3CH2)2CuLi CH2CH3 Wittig
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    Chad Notes.57.pdf

  • 1 pages Chad Notes.35.pdf

    Chad Notes.35.pdf

  • 1 pages Chad Notes.58.pdf
    • Chad Notes.58.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Hydride Reduction Reactions Summary Reduction of a ketone to a 2 alcohol O NaBH4 O EtOH . 1 LiAlH4 . + 2 H3O O Reduction of a aldehyde to a 1 alcohol O H O O Cl O O Reduction of a carboxylic acid to a 1 alcohol O OH Reduction of an amide to an amine O NH2
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    Chad Notes.58.pdf

  • 1 pages Chad Notes.52.pdf
    • Chad Notes.52.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Friedel Crafts Acylation (a phenyl ketone) and Formylation (benzaldehyde) O O Cl Cl R R AlCl3 AlCl3 Hydration of a Terminal Alkyne O HgSO4 H2SO4 . 1 Sia2BH THF . 2 H2O2, OH , H2O Grignard Addition to Nitriles . 1 CH3 MgBr R CN . 2 acid work up H O O R CH3
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    Chad Notes.52.pdf

  • 1 pages Chad Notes.47.pdf
    • Chad Notes.47.pdf
    • Lehigh University
    • Organic Chemistry I
    • CHM 110 - Fall 2014
    • Ortho/Para Directors (Activating except for halogens) -Halogens are deactivating ortho/para directors (pi donating but withdrawing inductively) Meta Directors (Deactivating) -Strongest donating group usually directs when there are competing substituents E
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    Chad Notes.47.pdf

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  • 27 terms

    Term:

    Biggest blood reservoir

    Definition:

    Veins

    • BIOE 210 - Exam #2
    • 27 terms
    • Vocabulary for BIOE 210 - Exam #2. Find, create, and access Study  questions, flashcards with Course Hero.

    BIOE 210 - Exam #2

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