Chem 210 reactions Study guides, Class notes & Summaries

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CHEM 210 Reactions Test Questions and Answers All Correct
  • CHEM 210 Reactions Test Questions and Answers All Correct

  • Exam (elaborations) • 3 pages • 2024
  • CHEM 210 Reactions Test Questions and Answers All Correct Describe the mechanism for the electrophilic addition of a strong acid. - Answer-Step 1) An alkene grabs a hydrogen off of a strong acid, forming a carbocation intermediate. Step 2) The conjugate base of the acid (an anion now) bonds to the open shell carbocation What is the regioselectivity of electrophilic addition reactions? - Answer-Markovnikov What is Markovnikov regioselectivity? - Answer-States that the major product is det...
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CHEM 210 REACTIONS EXAM  NEWEST QUESTIONS AND ANSWERS  (2023 / 2024) (VERIFIED  ANSWERS)
  • CHEM 210 REACTIONS EXAM NEWEST QUESTIONS AND ANSWERS (2023 / 2024) (VERIFIED ANSWERS)

  • Exam (elaborations) • 15 pages • 2024
  • What is the degree of substitution? <<ANSWERS>>>The number of alkyl groups a specific carbon is bonded to (more alkyl groups means more stable) What reagents are required in a dissolving metal reduction? <<ANSWERS>>>Na or Li, ammonia (NH3) as solvent Provide a summary of dissolving metal reduction <<ANSWERS>>>2 hydrogens (one equivalent) are added to an alkyne to form the E alkene (anti addition) What is the stereochemistry of the dissolving ...
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 PORTAGE LEARNING CHEM 210 exams 1-8 and final exam
  • PORTAGE LEARNING CHEM 210 exams 1-8 and final exam

  • Exam (elaborations) • 124 pages • 2023
  • Portage Learning CHEM 210 exams 1-8 and final exam Question 1 3 / 3 pts True or False: According to the Module, a compound with a molecular mass of 1,000 g/mol is considered a macromolecule. True Correct! False Question 2 3 / 3 pts True or False: Biomolecules can have only two functional groups. True Correct! False Question 3 3 / 3 pts True or False: The following functional group is an alcohol. True Correct! False Question 4 3 / 3 pts True or False: In ...
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CHEM 210 Final Exam Reactions, 2024.
  • CHEM 210 Final Exam Reactions, 2024.

  • Exam (elaborations) • 6 pages • 2024
  • CHEM 210 Final Exam Reactions, 2024. P450 [O] Breaks a double bond (even phenyl) to have add an oxygen that is bonded to each carbon of a double bond Rh/ Pt Dehydrogenation to form a double bond Br2 FeBr3 (cat) Adds a Br in the place of a hydrogen BH2-H Breaks triple OR double bond and adds H or BH2 to those carbons H2 NaNH3 Trans partial reduction of triple to double bonds H2 Lindrar's catalyst Cis partial reduction of
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Chem 210 Exam 4 Questions and Correct Answers, Complete Solution 2024.
  • Chem 210 Exam 4 Questions and Correct Answers, Complete Solution 2024.

  • Exam (elaborations) • 9 pages • 2024
  • Chem 210 Exam 4 Questions and Correct Answers, Complete Solution 2024. In order to make an alcohol we can do what types of reactions? addition reactions and oxidation reactions of alcohol What are the two types of addition reactions? hydration of alkene and addition reactions of H2 to C=O We need to figure out if alcohol is a... 1º, 2º, and 3º Ketone addition of H2 to make an alcohol is what type of alcohol? 2º Aldehyde addition of H2 to make an alcohol is what type of alcohol? 1...
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CHEM 210 Reactions Test Questions and Answers All Correct
  • CHEM 210 Reactions Test Questions and Answers All Correct

  • Exam (elaborations) • 3 pages • 2024
  • CHEM 210 Reactions Test Questions and Answers All Correct Describe the mechanism for the electrophilic addition of a strong acid. - Answer-Step 1) An alkene grabs a hydrogen off of a strong acid, forming a carbocation intermediate. Step 2) The conjugate base of the acid (an anion now) bonds to the open shell carbocation What is the regioselectivity of electrophilic addition reactions? - Answer-Markovnikov What is Markovnikov regioselectivity? - Answer-States that the major product is d...
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Portage Learning Chem 210 Module EXAM 8
  • Portage Learning Chem 210 Module EXAM 8

  • Exam (elaborations) • 12 pages • 2023
  • Portage Learning Chem 210 Module EXAM 8 Question 1 3 / 3 pts True or False: The majority of reactions of the urea cycle occur in the cytosol. Correct! True False Question 2 3 / 3 pts True or False: FADH2 yields 2.5 ATP molecules after donating electrons and hydrogen atoms to the electron transfer chain (ETC). True Correct! False Question 3 3 / 3 pts True or False: ATP is invested in the urea cycle. Correct! True False
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CHEM 210 Final Exam Reactions, 2024.
  • CHEM 210 Final Exam Reactions, 2024.

  • Exam (elaborations) • 6 pages • 2024
  • CHEM 210 Final Exam Reactions, 2024. P450 [O] Breaks a double bond (even phenyl) to have add an oxygen that is bonded to each carbon of a double bond Rh/ Pt Dehydrogenation to form a double bond Br2 FeBr3 (cat) Adds a Br in the place of a hydrogen BH2-H Breaks triple OR double bond and adds H or BH2 to those carbons H2 NaNH3 Trans partial reduction
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chem 210 exam 8 Questions and Correct Answers, Complete Solution 2024.
  • chem 210 exam 8 Questions and Correct Answers, Complete Solution 2024.

  • Exam (elaborations) • 7 pages • 2024
  • chem 210 exam 8 Questions and Correct Answers, Complete Solution 2024. T/F the majority of reactions of the urea cycle occur in the cytosol true T/F NADH yields 1.5 ATP molecules after donating electrons and hydrogen atoms to the electron transport chain (ETC) false T/F GTP is invested in the urea cycle false T/F there are six complexes associated with the ETC false T/F in the production of ATP via ATP synthase, the H+ ions move from the mitochondrial matrix to the intermembrane space...
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Chem 210 – Reactions Questions 100% Answered!!
  • Chem 210 – Reactions Questions 100% Answered!!

  • Exam (elaborations) • 6 pages • 2024
  • Chem 210 – Reactions Questions 100% Answered!! Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E...
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