Question: Please explain a step by step guide for being able to answer any E/Z configuration chemistry problem, finding the stereochemistry of stereo Centre, how many

Please explain a step by step guide for being able to answer any E/Z configuration chemistry problem, finding the stereochemistry of stereo Centre, how many configuration isomers and drawing syn and anti conformers as Newman projections and drawing most stable chair conformer of a molecule given as well as a guide covering any other topic so I can use it to answer any similar kind of question assume I know nothing about chemistry and act like ur trying to teach a 5 year old fully explain everything not just in a basic manner but to the furthest extent so I know what I'm looking for/ what todo as someone who knows NO CHEMISTRY I should be able to use this guide fully explaining these topics

to answer even the most difficult problem I have attached a problem of the level difficulty I should be able to solve these notes with and any other problem in my workbook that covers the same topics

review File Edit View Go Tools Window Help week 3 worksheet Page 9 of 11 week 3 worksheet (dragged).pdf 1 page Workshops Workshops WORKSHOP WEEK 3-Isomers WORKSHOP WEEK 2- Language of Chemistry 1. Consider the molecules (a)-(f) below. 1. Draw the following molecules as line structures. Br (a) ( b ) CH, CHCH3 (c) CH3CH=CCH,Br (8) CH,CHCCH2CH2OCH, (b) CH3CH=CHCH2CHO CH3 (d) - Br (e) CHICH=CBr2 Which one(s) can exist as E/Z isomers? Which ones can exist as R/S enantiomers? What is the stereochemistry of (a)? 2. Consider the structure shown right. List all the functional groups in the molecule. 2 Consider the molecule shown right. Classify the alkene as E, Z or neither E nor Z What is the stereochemistry of stereocentre (a) What is the stereochemistry of stereocentre (b) B How many sp2 carbons? Challenge: How many configurational isomers are 1 ( b ) there of this molecule? How many sp3 carbons? How many pi-bonds? 3. Draw both the syn and anti conformers of 2-methoxyethanol as Newman projections What's the molecular formula? (looking along the C1-C2 bond). Challenge: how many sigma bonds? 3. Consider the structure shown right. 4. Consider the structure, right: a. List all the oxygen-containing functional groups in the molecule. a) Is this cis, trans, E or Z? CH2OH b) Which of the structures below are conformers of the compound shown? c) Which of these is the MOST stable conformer of this molecule? OH How many sp2 carbons? CH2OH How many sp3 carbons? CO,H CH2OH CH2OH HOCH2OH d. How many pi-bonds? HO HO What's the molecular formula? D 5. Draw the most stable chair conformer of the molecule shown below. Explain why this Challenge: Where bonds have been drawn in 3D, draw in is the most stable conformer. the missing C-H bond, using appropriate 3D notation. Give the systematic (IUPAC) names of compounds (a) and (b) from Q1, and the compound in Q2 (challenge). " CHS OH

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