A-Level Chemistry - Organic Chemistry
15 cards in this deck
This free A-Level Chemistry deck covers A-Level Chemistry - Organic Chemistry, tagged for Edexcel. Every question in the deck is listed below — sign in free to flip each card, reveal the answer, and rate your confidence so spaced repetition can schedule your reviews for you.
All 15 questions in this deck
- What are the three stages of free radical substitution?
- State the conditions required for E/Z stereoisomerism to occur in a molecule.
- Explain Markovnikov's rule in electrophilic addition to unsymmetrical alkenes.
- Why do tertiary halogenoalkanes react via an SN1 mechanism rather than SN2?
- What reagents and conditions are needed to fully oxidise a primary alcohol?
- Describe the observation and species formed when an aldehyde is warmed with Tollens' reagent.
- What is the purpose of reacting a carbonyl compound with Brady's reagent (2,4-DNPH)?
- Why is benzene's enthalpy of hydrogenation less exothermic than the Kekulé structure predicts?
- Give the equation for generating the electrophile in the nitration of benzene.
- Explain why acyl chlorides are much more reactive than carboxylic acids.
- What is a racemic mixture and why is it optically inactive?
- Why is ethylamine a stronger base than ammonia?
- What is a zwitterion in the context of amino acids?
- Name the two types of monomers required to synthesize the polyamide Kevlar.
- In proton NMR spectroscopy, what does the splitting pattern of a peak indicate?
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Frequently asked questions
How many flashcards are in A-Level Chemistry - Organic Chemistry?
This deck contains 15 flashcards, each with a question on the front and the answer on the back. All the questions are listed on this page — create a free account to flip the cards and see the answers.
Is this A-Level Chemistry deck free to study?
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Which exam board is this deck for?
A-Level Chemistry - Organic Chemistry is tagged for Edexcel. Check your specification if you study with a different exam board — core content often overlaps.
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