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- Organic Chemistry 1. Can you please explain all three answer choices ? Why is it ! and III, and not II ? Thank youPlease show the steps to the organic synthesis reactions below:I put in the answer for compound A, (dimethyl‐lambda4‐sulfanylidene)cyclopropane, and the product 9‐oxadispiro[2.0.44.13]nonane, in the boxes, but it says it's incorrect. What am I not getting?Thank you for your help!
- Which of the following is the most volatile? 1-ethoxypropane (MW = 88) 1-pentanol (MW = 88) 1- aminopentane (MW = 87) butanoic acid (MW = 88)Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation. My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???How would the following conversion be achieved? Please show the reaction mechanism step by step
- 3 Organic chemistry, Q: Explain to thoroughly (pretend i'm completely new to the subject) with text and if needed drawings the chemistry of the carbonyl group, direct addition of nucleophiles and addition with elimination No short answers pleasePossible route of synthesis to this reaction. Example: 1) Br2; H2O 2) H2SO4, H2O2. What reaction conditions would you use to carry out the following conversions. Note include all steps of the reaction including work up as necessary.