Nabh4 - Study guides, Class notes & Summaries

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Organic Chemistry 202 Synthetic Transformations, Top Exam Questions & answers, Rated A+
  • Organic Chemistry 202 Synthetic Transformations, Top Exam Questions & answers, Rated A+

  • Exam (elaborations) • 6 pages • 2023
  • Organic Chemistry 202 Synthetic Transformations, Top Exam Questions & answers, Rated A+ reduction of an aldehyde or ketone to an alcohol LiAlH4 or NaBH4 H3O H2O lithium dialkyl cuprate reagent from an alkyl halide 4 Li metal CuI reduction of a nitro group to an amine Zn(Hg) HCl reduction of a benzyl carbonyl H2/Pd or Zn(Hg) HCl NAS (normal condition must be 1 EWG ortho/para to leaving group) nucleophile (–OH, –OR, R3N) benzyne reactions 1) NaOH 2) dilute acid benzyne...
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OAT exam And Complete Answer.
  • OAT exam And Complete Answer.

  • Exam (elaborations) • 2 pages • 2024
  • henderson hasselbach equation: - correct answer pH = pKa + log ([conj. base]/[weak acid]) pOH = pKb + log([conj. acid]/[weak base]) percent comp by mass (solution) = - correct answer mass solute / (mass solute + solution) mole fraction = - correct answer moles of compount / total moles in system molarity = - correct answer moles solute/liters solution molality = - correct answer # moles of solute / kg of solvent normality = - correct answer # of equivalents of solute / liters o...
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Unit 3 :CHEM 210 with 100% correct answers
  • Unit 3 :CHEM 210 with 100% correct answers

  • Exam (elaborations) • 4 pages • 2023
  • Bronsted-Lowry Acid Must Have a Proton (H) Bronsted-Lowry Base Must have Lone Pairs or Pi Bonds Neutralization Strong Acid donates a proton to the Strong Base to generate Water and the Conjugate Base Electrophile Electron Loving An atom that wants electrons. An atom that is electron rich. Must have a partial positive charge. (Cation) Nucleophile Nucleus Loving If opposites attract, then a _________ is electron rich. Must have a partial negative charge. (An...
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OCR A-Level Chemistry A Organic Synthesis Question 100% solved
  • OCR A-Level Chemistry A Organic Synthesis Question 100% solved

  • Exam (elaborations) • 3 pages • 2023
  • OCR A-Level Chemistry A Organic Synthesis Question 100% solvedAlkene + hydrogen /nickel catalyst/423K= alkane Alkene + bromine /room temperature= dihaloalkane Alkene + HCl(g/aq) /room temperature= haloalkane (mixed products) Alkene + H2O(g) /H3PO4= alcohol (mixed products) Primary alcohol + 2[O] /excess K2Cr2O7/H2SO4/reflux= carboxylic acid Primary alcohol + [O] /K2Cr2O7/H2SO4/distil= aldehyde Secondary alcohol + [O] /K2Cr2O7/H2SO4/reflux= ketone ...
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Orgo 2223B final-lipids Summary Questions and Answers
  • Orgo 2223B final-lipids Summary Questions and Answers

  • Exam (elaborations) • 5 pages • 2023
  • Orgo 2223B final-lipids Summary Questions and Answers Are lipids soluble or insoluble in water? - CORRECT ANSWER-insoluble What type of double bonds do naturally occurring fatty acids have? - CORRECT ANSWER-cis When fatty acids are added to water, do the majority of them remain ionized or nonionized? - CORRECT ANSWER-nonionized What is the name of the reaction for the synthesis of fatty acids? - CORRECT ANSWER-Claisen condensation What type of reaction is a Claisen condensation? - C...
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AQA A-Level Organic Synthesis Latest 2023 Already Passed
  • AQA A-Level Organic Synthesis Latest 2023 Already Passed

  • Exam (elaborations) • 6 pages • 2023
  • AQA A-Level Organic Synthesis Latest 2023 Already Passed Alkane to Halogenoalkane X2, UV light Mechanism = free radical substitution Halogenoalkane to Alkene KOH, dissolved in ethanol and heated under reflux Mechanism = Elimination Alkene to Halogenoalkane HX at room temperature Mechanism = Electropholic Addition Halogenoalkane to Alcohol Warm NaOH/KOH, heated under reflux Mechanism = Nucleophilic Substitution Halogenoalkane to Nitrile KCN, dissolved in ethanol and heated under reflux Mechan...
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Chemical properties of Aldehydes and Ketones
  • Chemical properties of Aldehydes and Ketones

  • Exam (elaborations) • 83 pages • 2024
  • Chemical properties of Aldehydes and Ketones in of Electrons Loss of Electrons H O H3C C H + 2[H] H3C C OH H True for all secondary alcohols Carbonyl + 2[H] ─(NaBH4) Alcohol CH3CH2CHO + 2[H] CH3CH2CH2OH Propanal + NaBH4 Propan-1-ol
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Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ket
  • Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ket

  • Exam (elaborations) • 45 pages • 2024
  • Chemical properties of Aldehydes and Ketones Reactions common to both Aldehydes and Ketones The difference between an Aldehyde and a Ketone is the position of the C=O (Carbonyl group). Aldehyde – always on a carbon at the end of the chain Ketone – Always on a carbon at middle carbon of the chain 1. BOTH Aldehydes and Ketones can be reduced Aldehyde reduced to Primary Alcohol Reducing agent = Sodium tetrahydroborate III (NaBH4) Ketone reduced to Secondary Alcohol Reduction Oxidisatio...
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chem 219 module 6 exam with complete solution
  • chem 219 module 6 exam with complete solution

  • Exam (elaborations) • 10 pages • 2024
  • R-NH2 R-NH2 Choose matching term 1 primary amine 2 higher than alkanes lower than alcohols 3 two main steps of reductive amination? 4 cyclohexylamine Don't know? Terms in this set (124) Original amine derivative of ammonia where one or more hydrogen replaced by carbon-based groups primary amine R-NH2 Previous Play Next Rewind 10 seconds Move forward 10 seconds Unmute 0:01 / 0:15 Full screen Brainpower Read More secondary amine R2NH tertia...
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Chem 210 Module 7 Exam (2023/2024) Newest Questions and Answers (Verified Answers)
  • Chem 210 Module 7 Exam (2023/2024) Newest Questions and Answers (Verified Answers)

  • Exam (elaborations) • 3 pages • 2023
  • Chem 210 Module 7 Exam (2023/2024) Newest Questions and Answers (Verified Answers) Strong oxidants - ANSWER️️ KMnO4, CrO3 mild oxidants - ANSWER️️ PCC, O3 strong reductants - ANSWER️️ LiAlH4, NaBH4, H2 (Pt or Lindlars), Na/Li NH3, H2SO4, BH3 primary alcohol to carboxylic acid (oxidant) - ANSWER️️ CrO3 primary alcohol to aldehyde (oxidant) - ANSWER️️ PCC aldehyde to primary alcohol (reductant) - ANSWER️️ NaBH4 aldehydes to primary alcohol, carboxylic acids to prim...
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