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Redox
AndyelAndyel

Redox

(0)
Recap/Revision lessons with a focus of constructing half equations and REDOX equations.
Titration and standard solution - required practical
AndyelAndyel

Titration and standard solution - required practical

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Describe how to prepare a standard solution of sodium hydrogensulphate. Suggest suitable techniques that will help a student to carryout an accurate titration. Development of exam technique when approaching titration how science works questions
Group 7 Halogens
AndyelAndyel

Group 7 Halogens

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Describe the trend in boiling points and oxidising ability of the halogens. Predict observations for a displacement reaction between aqueous halogens and aqueous halides. Construct equations for chlorine disproportion chemistry
Aldehydes and ketones
AndyelAndyel

Aldehydes and ketones

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Recall how alcohol FG can be oxidised into carbonyl containing FG. Identify a suitable reducing agent for reducing a carbonyl into an alcohol. Construct a mechanism to show the reduction of a carbonyl. Explain how racemic mixtures can be formed.
Redox equation activity
AndyelAndyel

Redox equation activity

(0)
Structured activity that allows student’s to apply their knowledge and understanding of REDOX chemistry.
Determining the pKa of aspirin:  Required practical
AndyelAndyel

Determining the pKa of aspirin: Required practical

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Calculating the pH of a weak acid. Describe how to produce a standard solution. Propose a suitable experimental method that could be used to determine the pKa of aspirin. Use Excel to create a calibration curve and to generate a calibrated data set. (Included) Analysis of a pH curve to determine pKa.
Revision: Transition metals
AndyelAndyel

Revision: Transition metals

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Describe the features of a complex ion. Explain how a complex is coloured. Determine the formula of a complex using colorimetry. Determine the concentration of a complex using colorimetry and titrations.
Revision: Alkenes
AndyelAndyel

Revision: Alkenes

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Describe E/Z stereoisomerism. Explain how to use CIP rules to classify an isomer E or Z. Recall polymerisation of alkenes Outline the two mechanisms that alkenes undergo and justify why the major product is formed.