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- chemist wants to perform a reaction using the reagent below, which can act as a Brønsted-Lowry base. Considering only the reagent's capacity to act as a base, check the boxes of any compounds in the table that the chemist should not use as the solvent for the reaction. Use the ALEKS Data resource to look up useful data. If all of the solvents below are acceptable, please check the box that says "All solvents are acceptable." All solvents are acceptable reagent 人。 ONa proposed solvent H N - CH, NH, do not use this solvent (check all that apply) ☐ ☐ ☐chemist wants to perform a reaction using the reagent below, which can act as a Brønsted-Lowry base. Considering only the reagent's capacity to act as a base, check the boxes of any compounds in the table that the chemist should not use as the solvent for the reaction. Use the ALEKS Data resource to look up useful data. If all of the solvents below are acceptable, please check the box that says "All solvents are acceptable." All solvents are acceptable proposed solvent do not use this solvent (check all that apply) reagent NaSH i H₂O ΝΗ, メ OH ☐ ☐ ☐help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working
- (2) Chemistry ........can someone help me I figured the Br would be left and I would go with Na and then the bottom reactant would give a double bond. The second reaction I am a little lost on as well.Examine the molecules below. Which site is most basic? Which H is most acidic? Highlight this site. Highlight this H. H :S- H. :O:
- achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3e. f. Br NaH SH 1. PBr3 2. Mg, thf 3. Ethylene oxide 4. H₂O/H3O+ Label step 3 only OHdont want hand writting image i will dislike you in 10 accounts
- NoneIn the following acid-base reactions, 1. draw Lewis structures of the reactants and the products. 2. determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). 3. use the curved-arrow formalism to show the movement of electron pairs in these reactions, as well as the imaginary movement in the resonance hybrids of the products. 4. indicate which reactions are best termed Brønsted-Lowry acid-base reactions. (c) -BH₁₂ BH3 + CH3-O-CH3 → CH3-O-CH3 (d) 유 0- CH3-C H + -OH CH₁₂-C-H OH.CI 1.) Me CuLi 2)LDA 3.) a) 1.) b.) 1.) c.) 1.) 2) 2) 2) 0 O. 3.) 3.) 3) R R d) 1.) e) 1.) R. R. 2) 2) 3.) 3.) "R"abbreviatian for answers
