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- Draw the structure of the major organic product of the reaction. 1. LIAIH4, ether 2. H₂0 ● You do not have to consider stereochemistry. Submit Answer ***I Q CI / Retry Entire Group [ ] در ? ChemDoodleⓇ [F 3 more group attempts remaining view Topics] [References]Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?149) Why is a tertiary alcohol more reactive with hydrogen halides, than secondary alcohols? Because secondary alcohols are smaller and therefore less reactive for the attack of halide nucleophile. Because tertiary alcohols have more hydrogen atoms available for substitution reactions. Because a tertiary alcohol can form a more stable carbocation as an intermediate in the reaction. Only the 1st and the 2nd statements are acceptable.
- A. REACTIONS OF ALKENES- provide the product(s) or reagents that are needed to accomplish the following transformationsPlease help with the following OChem reaction sequence... What is the major product obtained from the following reaction sequence? Also provide the structures for the major organic products formed in each step A, B, C, and D (see attached image)Write step-by-step mechanism for the following rearrangement: он H,SO, H,SO, Он ........... .............. **.*......
- Consider the reaction below: Br H₂O heat OH to 1. The reaction mechanism for the reaction is choose your answer... 2. The nucleophile in the reaction is a choose your answer... ✓nucleophile.Draw the structure(s) for the major organic product(s) of each of the following reactions or write N.R for No Reaction. Draw the correct stereochemistry when necessary КОН MEOH DMF CI ..... t-BUOK MeONa THE THE heat heatUse the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaCN Br CN CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaCN X: choose your answer... Y: choose your answer... Z: choose your answer... >
- Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous NextMatch the following corresponding carbons in the reactants and product to the net reaction at that carbon. Answers may be repeated. 0 0 00 0 0 H Choose... Choose... AWhich rearrangement would the two example of carbocation below most likely undergo? a. Methyl shiftb. Hydride shiftc. Paradigm shiftd. Equilibrium shift
