This summary outlines the experiments and topics that will be assessed in Lab Quiz 1, providing an overview of key areas of focus and sample question types.
Experiment 1: Properties of Hydrocarbons
Focus: Understanding polarity, solubility, and reactivity of hydrocarbons, specifically alkanes, alkenes, and aromatics.
Reactions Studied:
Bromination: Addition reactions involving bromine.
Permanganate Oxidation: Reaction of hydrocarbons with potassium permanganate (KMnO4) to assess their reactivity.
Experiment 2: CO2 Extraction of Limonene
Focus: Understanding phase diagrams and the extraction process of limonene using CO2.
Experiment 3: Synthesis of Aspirin
Focus:
Determination of molecular formula and calculations of molar mass.
Calculating moles from mass and vice versa.
Calculating percent yields.
Experiment 4: Functional Groups Worksheet
Focus: Identifying various functional groups covered in class:
Alkene/Alkyne
Alcohol
Aldehyde/Ketone
Carboxylic Acid
Ester
Amine/Amide
Experiment 5: Properties of Analgesic Drugs
Focus:
Examining NSAIDs and their mechanisms of action.
Assessing solubility and pH properties.
Experiment 6: Esters and Soaps
Focus:
Predicting products of condensation, hydrolysis, and acid/base reactions.
Identifying amphipathic compounds.
Experiment 7: Characterization of Carbohydrates
Focus: To be determined (TBD).
Matching Compounds with IUPAC Names:
Identify major functional groups for listed compounds:
a. Butan-2-one
b. Buta-1,3-diene
c. Benzene
d. Methanal
e. Hexane
Reactivity Ranking:
Rank the reactivity of alkanes, alkenes, and aromatics from least to most reactive based on potassium permanganate reactions.
Addition Reactions:
Identify types of compounds that participate in addition reactions based on previous rankings.
Markovnikov’s Rule:
Understand how this rule predicts products in addition reactions, summarized as "the rich get richer and the poor get poorer."
Application: Determine the product of a specified addition reaction using this principle.
Acetaminophen Synthesis:
Calculate the molecular formula and molar mass for p-aminophenol and acetaminophen.
Theoretical yield calculation:
Given 2.4 grams of p-aminophenol, calculate the theoretical yield of acetaminophen.
Percent yield calculation:
If 1.7 grams of acetaminophen are prepared, calculate the percent yield.
Discuss the possibility of achieving over 100% yields in class experiments and analyze reasons behind this phenomenon.
Mechanism of Action for Acetaminophen and NSAIDs:
Discriminate among potential mechanisms of action, including:
Inhibition of COX-2 enzymes
Interaction with mu-opiate receptors
Hydrophobic interactions with nonpolar materials.
Ester Formation:
Identify the ester formed from a specified reaction.
Saponification Process:
Understand the reaction processes involved in saponification of triglycerides, identifying the sequential reactions in this context (acid/base and hydrolysis or condensation).
Amphipathic Compounds:
Define amphipathic compounds and discuss their characteristics, particularly their dual affinity towards polar and nonpolar environments.
Analgesic Drug pH Prediction:
Predict whether ibuprofen, aspirin, and acetaminophen are acidic, neutral, or basic based on pH tests.
Conjugate Bases of Acidic Analgesics:
Illustrate the conjugate base for those analgesic drugs expected to be acidic post-reaction with sodium hydroxide (NaOH).
Matching Compounds with IUPAC Names:
a. Butan-2-one: Ketone
b. Buta-1,3-diene: Alkene
c. Benzene: Aromatic hydrocarbon
d. Methanal: Aldehyde
e. Hexane: Alkane
Reactivity Ranking:
Alkanes (least reactive) < Alkenes < Aromatics (most reactive) based on potassium permanganate reactions.
Addition Reactions:
Compounds that participate: Alkenes and Aromatics based on previous rankings.