7. I can do organic conversions to get from one molecule to a different one.

A = 1 step

M = multiple steps

E = full conversion

FYI - The conversion organic questions are also hard to teach and there isn't a set section in the sciPAD that covers it. The best way to learn it is by memorizing the tests and doing practice questions. 

1. Do Now (Day 1) - Draw the following two molecules: propanone and ethyl propanoate. 

2. Ms Garlick will do the 2021 Question 2c as model answer. "Devise a reaction scheme to convert propanone into ethyl propanoate." Remember that for each step there needs to be the reagents and conditions, plus structural formula for the organic product after each step.

3. Mahi Choice - pick from the following options something to work on based on where you are in your learning of reaction schemes/conversions. 

   1. • Memorize the conversion reactions with Quizlet or using the No Brain Too Small Conversion Flash Cards

      • Just the L3 Organic Reaction Scheme Blank to start making summary notes. 

      • sciPAD pages 

        1. • Addition Reactions - Hydrogenation (page 15/127)

           • Addition Reactions - Halogenation (page 16/128)

           • Addition Reactions - Hydrohalogenation & Markovnikov's Rule (17-18/129-130)

           • Saytzeff's Rule - Elimination Reaction (Page 19-20/131-132)

           • Hydrogenation of Alkenes (page 21-22/133-134)

           • Lucas' Reagent (page 38/150)

           • Alcohols to Chloroalkane & Converting Alcohols to Chloroalkane (page 40-42/152-154)

           • Haloalkanes to Alcohols (pages 46-47/158-159)

           • Elimination Reactions - Alcohol to Alkene (page 48/160)

           • Elimination from Alcohols - Saytzeff's Rule (page 49/161)

           • Addition Reaction - Making Alcohols by Hydration (page 50/162)

           • Reactions of Alcohols - Oxidation (page 53/165)

           • Alcohols from Aldehydes & Alcohols from Ketones (page 58/170)

           • Summary of Reactions (page 61/173)

           • Haloalkanes to Amines (page 70-71/182-183)

           • Carboxylic Acid Derivatives - Acid Chlorides (page 75/187)

           • Reactions of Acid Chlorides (page 76/188)

           • Reaction with Ammonia (page 77-78/189-190)

           • Reaction with Primary Amines (page 79-80/191-192)

           • Esters (page 84-85/196)

           • Esters from Acid Chlorides (page 87/199)

      • Work on the No Brain Too Small Collated Reaction Schemes & Conversion Question (skip the conversion questions, we'll cover that in the next lesson, just focus on things with boxes)

      • Work on "CPR" Quiz 7 - Conversions (Answers)

4. Do Now (Day 2) - Make a SMART goal for this session. 

5. Continue with Mahi Choice.

"CPR" Quiz 7 - Conversions (Answers)