please show mechanism and product. i keep getting stuck, is there supposed to be a carbocation...
I keep getting stuck in the process please show me step by step thank you
2. Draw the product of a carbocation rearrangement for the carbocation A shown and provide a complete step-by-step mechanism for the rearrangement (show all relevant hydrogens, curved arrow(s) and indicate the position of the charge(s)). Also, if applicable (!), draw one additional resonance structures for the product of the rearrangement. product of the rearrangement additional resonance structure (if possible) SA redraw A with all relevant Hydrogens
Please help me with the following organic chemistry chapter 7 questions. I keep getting them wrong and I don't know why. Draw a structural formula for the major organic product of the reaction shown. CH3CH2CH2CH2CH3 + нан HI Draw a structural formula for the major organic product of the reaction shown. CH3 [ CH3 + HCI → Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown. HOD. + HI H3C
What is the mechanism needed to produce the given product? How does a carbocation rearrangement (acidic mechansim) give rise to the product? Hint: Disconnection and ether synthesis in acidic/basic conditions. u poc
the correct answer to #11 is supposed to be b but i keep getting c. what am i doing wrong? also, the correct answer to #14 is b but i keep getting d. please explain where i am going wrong. thank you 11. Consider the reaction in the previous question, what the equilibrium constant would be equal to at 25°C? a) 0.645 AGE-RT enk b) 1.03x10-16 c) 9.64x10-1. 91.2-0008314 (298,15) enk d) 7.03x108 -0.036B-Ink 12. When a reaction is found...
the duulatur nucleophile after rearrangement. This is the pluu If the carbocation Is captured by the is captured by the nucleophile before rearrangement. The product distribution (ratio of products) depends on how fast the rearrangemen how fast the nucleophile attacks the carbocation. If the rearrangement occurs faste the nucleophile, then the rearranged product will predominate. However, if the nu the carbocation faster than rearrangement (if it att Gent Gif it attacks before rearrangement occurs), th arranged product will predominate. In...
Keep getting stuck on 7-34 . Can someone please solve for the displacement and slope at A by using the moment area theorems? ine the maximum displacement of the beam 7 at A. El is constant. Use the moment-area A rems th Ive Prob. 7-34 using the conjugate-beam method. 30 kN m 6 m Probs. 7-34/35
Can someone please help me? I keep getting stuck, I don’t know how to get log on the other side of the equation. I can easily follow another tutorial, but I can’t figure out the ending and what step I need to do to get it! This was previously answered by someone else and was wrong. I need to know HOW to work it out please! Given the measured cell potential, Ecel, is-0.3555 V at 25 C in the following...
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
This is an acid catalyzed dehydration of alcohols mechanism that I am supposed to provide the product for and I do not understand the steps any help would be appreciated. This is supposed to be an E1 reaction 2 Мео H2SO4 heat ni