(c) Use what you learned in Question 2 to illustrate each type of force that can exist between two methanol molecules. Hint: you have done this quite a bit already in lab and lecture. London Dispersion Dipole-Induced Dipole Dipole-Dipole Hydrogen-Bonding
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- Need help solving this, please show your work with the answer!When drawing the resonance structures for a toluene carbocation (like the one attached below), should I include the structure created after a bond shift from the fourth structure, even though it mimicks the first structure? What about in the second picture- should the crossed out structure be included despite its similarity to the first one? Overall, I'm having trouble determining whether two compounds are the same and don't need to be drawn twice or just similar and need to drawn twice.Please answer all part of the question...thank you
- Solution plz with explanation, should correctCan i get help with problemDraw the structure(s) of the major organic product(s) of the following reaction. Aqueous NaHCO3 + • You do not have to consider stereochemistry. If there is more than one major product possible, draw all of them. • If no reaction occurs, draw the organic starting material. **** 1 eq. Br₂ Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. 8 ChemDoodle Sn [F
- pls answer them all with detailed explanation/s, thank you!practice q 13 13. Complete each of these following reactions (i.e. fill in the boxes with the missing reagent(s) or major product(s). Indicate the stereochemistry if applicable.1ormula of eacn. (a) (b) H. NH2 Oseltamivir Clopidogrel (Plavix) (Tamiflu) General Problems Why do you suppose no one has ever been able to make cyclopentyne as a stable molecule? 1-46 Cyclopentyne Copyright 2016 Cengage Learning. All Rights Reserved. May not be copied, scanned, or duplicated, in whole or in part. Due to electronic rights, some third party content may be suppressed f torial review has deemed that any suppressed content does not materially affect the overall leaning experience. Cengage Leaming reserves the right to remove additional content at any time if HAPTER 1 STRUCTURE AND BONDING Allene, H2C=C=CH2, is somewhat unusual in that it has double bonds. Draw a picture showing the orbitals invo and 7 bonds of allene. Is the central carbon atom sp2- or sp What about the hybridization of the terminal carbons? W you predict for allene? 1-47 Allene (see Problem 1-47) is structurally related to car CO2. Draw a picture showing the orbitals involved in the c of CO2, and identify…
- The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs o the weakest C-H bond. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. Separate resonance structures using the symbol from the drop-down menu. Include all valence radical electrons in your answer. 000 PreviousC Chemistry nardi and Neil Schore presented by Sap Propose an efficient synthetic scheme for the conversion of lactone A into amine B, a precursor to the naturally occurring monoterpene C. Note: If one or more reagents are incorrectly placed, a single red X will appear on the top left. C CHs CHs CH3 2. CH3 H3C CH3 H3C CHs CH3 H3C CH но но 3. CH3Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations are not needed. Keep it short, brief, and direct because I only need the answers as soon as possible. Determine the number of stereogenic centers in 3,4,5,6-tetraethyldecane. a. 1b. 2c. 3d. 4