Topic: Organic Chemistry
Please provide step by step solutions to each problem along with a brief explanation as to why you picked your answer.
To whoever helps me, please know that I am stuggeling so hard with this class. I'm not smart like everyone else, so please (if you can) be detailed and if you have time, please try to explain to me why you did what you did. I just don't get this subject, it seems so random and people skip so many steps so I cannot follow. Please help. Thank you so much.
therefore the complete name for compound b is 2E,4E-6-methylocta-2,4-diene.
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Topic: Organic Chemistry Please provide step by step solutions to each problem along with a brief...
Topic: Organic Chemistry Please provide a neatly drawn, detailed answer showing step by step solutions. Thank you for your time and help. 6. Use your knowledge of fused-ring systems from lecture, as well as principles of conformational analysis and your molecular model kit, to draw the most stable conformation of the steroid shown below. You do not need to worry about the conformation of the 5-membered ring. он HIH но
Topic: Organic chemistry, nucleophilic substitution (R)-2-butanol is labelled with O-18 and participates in the following reactions: What is the final configuration of the product? Explain. (I'm confused in this subject so please leave a detailed explanation) он 18OH + (CH3SO2-018) CH SO2C CH3CH2CHCH3 dioxane CH3CH2CHCH3 CH3CH2CHCH3
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. 4. Provide a complete curved-arrow mechanism for the transformation shown below. You do not need to account for any stereochemistry in your mechanism NH2 Me Me HO Ph Мео pH 5 O Ph
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. 6. As you have seen in lecture, acid halides react with alcohols to form esters. a. Provide a complete curved-arrow mechanism for the following transformation of an alcohol into an ester. HO HO rox b. In the above transformation, only one of the two hydroxyl groups in the starting material was successfully acylated under the given conditions. Provide...
several types of reactions organic chemistry Please reflect on the reactions in organic chemistry 1, and choose an area that you would like to study at a more advanced level. Explain why your chosen area interests you. Would more advanced knowledge in this specific area relate to your future goals? can someone help me write about this topic, please!! I want different ideas other than what has answered previously
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. Each of the following transformations can be carried out in no more than three steps. Fill in the reagents required 3. for each step. If a step is not needed, mark an X for that step. а. 1 2. 3. b. 1 NEt2 2. 3. C. 1 он OPh Н. н 2. 3. d. OH 2. 3. е....
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. 1. Provide the missing starting material for each of the following transformations. There may be multiple possibilities for a particular sequence of reactions, but you need only provide one correct answer to receive full credit. 1. NH3, pyridine 2. LAIH, Et20 3. H+ workup b. 1. H30* 2. SOCI2 3. EtOH C. N-CH3 1. CrO3, pyridine I 2....
Please show me the following mechanism step-by step without missing any arrows. I've tried a few times and I'm a bit confused. This is between 5-nitro-2-furaldehyde in 12 mL distilled water and aminoguanidine bicarbonate in distilled water. I have added pictures of each one. Please be confident in your mechanism. Thank you very much. Please don't skip any steps. I'm struggling so much, if you skip steps ill never know what is going on. Thank you. 49 mg of aminoguanidine...
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products along with brief explanations. Thank you. 5. Carbamate esters are esters that bear a nitrogen group, but in many respects they behave exactly as one would expect of regular esters. Provide a complete curved-arrow mechanism for the following transformation of a carbamate ester, being sure to account for the observed deuterium label in the products 1. LIAID4 (excess), Et2o CF3 CF3 N DзC-он +...
Hi I need help with my homework I provide with the topic and the material please be clear and put it under each point please be clear make sure no plagiarisms write for each point please give good essay please help me I need it now "Maestro: A Surprising Story About Leading by Listening, by Roger Nierenberg STEP TWO: READ your shiny new (to you) book and absorb the many leadership lessons throughout :) STEP THREE: WRITE a 1-page reflection...