Draw the curved arrow notation and predict the products when one equivalent of hydroxide in DMSO at room temperature is added to 5-bromo-1-iodopentane. i DMSO + Br i i iDraw the major organic product with lone pair electrons
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- 1. Which absorbs at higher frequencies: a C-H or C-D bond? Explain. 2. Predict which alkene will predominate at equilibrium. Explain.Draw the curved arrow mechanism for the reaction between (2R,3S)-3,5-dimethylhexan-2-ol and PCl3. Note the specific instructions for each box. Include nonzero formal charges and lone pairs of electrons on all appropriate atoms. Then answer the question about the mechanism.for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow mecanism. based on the reaction products, explain why a carbocation intermediate cannot be proposed
- Using Curved Arrow Formalism, draw the reaction of 1-methylcyclopentanol treated with aqueous sulfuric acid and identify the rate determining step. If more than one product is formed, identify which is major, minor, very minor, etc. Thank you for the help with this question. I appreciate it.Complete the following reactions by drawing the major product (sfor each of the following reactions. Unless specified, assume there is only on equivalent of the reactants.d) Please correct answer and don't use hend raitingFor eaach image, predict the MAJOR product(s). Show stereochemistry where applicable and draw out ALL stereoisomers formed (as major products) in each reaction. State the mechanism(s) by which the major product(s) are formed (SN1, SN2, E1, and/or E2). Reagents are NOT present in excess.
- Determine and draw the product of the following reactrans ,write in any added hydrogens. 1,2,3,4,1bDraw the mechanism for the following reaction: Hint: the addition Br2/H2O to alkynes follows an analogous pathway as with the alkenes.Draw the missing major organic product(s) for each of the following reactions (do not write “+ en” as a product and remember stereo- and regiochemistry!). If no reaction occurs, write “NR”.
- Please solve correctly with explanation also. (Gpt/Ai wrong answer not allowed) Q. what is the product produced when 2-methyl-3-bromohexane reacts with tert-butoxide(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, andthe products. Note that the initial product is the salt of an amine (RNH3+ Br - ), which is deprotonated by the excess ammonia to give the amine.The iodination of acetovanillone (1-(4-hydroxy-3-methoxyphenyl)ethan-1-one) occurs in the following reaction: C9H10O3 + NaI + NaOCl --> C9H10O3I + NaCl Draw the complete reaction mechanism of acetovanillone including curved arrows.