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- Help me please on both , for the second pic is more: f. CH4 g. H2O h. CH3ClAnswer the following: How many H? Most polar bond? Least polar bond?Help! a.) Draw all the important resonance contributors for the structure shown below. Use curved arrows to show the movement of electrons between these contributors. b.) Draw the hybrid resonance hybrid structure.
- Why are the two resonance structures I circled in green incorrect? My professor's answer key is the picture with the red text.Hw problem wants 2 structures that have the same molecular formula but different connectivities for C3H4Below is the SN2 reaction between iodocyclohexane and cyanide (CN–). Draw the missing curved arrow notation in the first box to reflect electron movements. In both boxes, add lone pairs of electrons and nonzero formal charges.
- Diazomethane has the formula H2CN2. Draw all valid resonance contributors for diazomethane and, using Table 1-3, propose which one contributes more to the resonance hybrid. Hint: There are no structures that avoid charged atoms.VISUAL SKILLS The isomers of retinal have the same number of atoms and bonds but differ in thespatial arrangement at one carbon-carbon double bond (C“C). In each isomer, circle that C“C. Lookingat the atoms around that bond, to what atoms do the terms cis (same side) and trans (opposite side) refer?What is the dash formula of CH3CH2CH(NH2)CH3. Expand the following condensed formula so as to show all the bonds and unshares electrons.
- What's the steric number , electron paid geometry, number of lone pairs, molecular geometry, and hybridization for Boron Trichloride hexachlor bismuthate (III) Bromine Pentafluoride and carbon tetrachloride answer all please and please label so I know which is which just give me answers no extra stuff neededFor problem 3, why does N keep its electrons in addition to taking the H+ from the other molecule? Didn't it give its electrons to the other molecule?Homework problem wants to different structures that have the same molecular formula but different connectivities for c5h12