Please explain In detail why the solution is A 16. What is the molecular formula corresponding...
Please explain these ozonolysis probelms The alkene shown below is treated sequentially with ozone (O3) and zinc/acetic acid. Draw structural formula(s) for the organic product(s) formed. The alkene shown below is treated sequentially with ozone (O3) and zinc/acetic acid. Draw structural formula(s) for the organic product(s) formed. An alkene having the molecular formula C8H12 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. Draw a structural formula for the alkene.
16. What is the molecular geometry of the bromate ion, BrO3–?Please explain whyA) square planarB) trigonal planarC) square pyramidalD) tetrahedralE) trigonal pyramidal
4. Draw the structural formula corresponding to each of the follow ach of the following molecular models. moodi v sambo onde den s o bado boods (b) d own boods 5. Draw the electron dot formula corresponding to the structural formula of the above models. Hol o tto dobod to the bodo (a) badoo lo lodo volalo a bs (0 obrodotto bot t es motos de brod siduob brodova nontologonlobood plantsumo con lot no toplo ponovo dun sabong bass boog...
First, using the molecular formula of C7H10BrFS please DRAW a bond-line structure and the corresponding 1H NMR spectrum. Second, using the same molecular formula, please draw a constitutional isomer and the corresponding 13C NMR. Please be sure to have both representations properly drawn as well as the corresponding spectra.
Write the structural formula of a compound of molecular formula c4h8cl2 in which a) All carbons belong to methylene groups b) None of the carbons belong to methylene groups Please explain why you wrote the structures the way you do
Can you please explain, in detail, how to draw a 1H NMR and 13C NMR spectrum from a bond-line structure. Molecular formula is C7H10BrClS, please convert to bond-line structure for corresponding spectrums.
please explain all answers! MC.4 A compound X with molecular formula CgHı2 and no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula C2H4. What can be said about the structure of compound X? A) Compound X has 3 rings. B) Compound X has 1 ring and 2 double bonds. Compound X has 2 rings and 1 double bond. Compound X has 3 double bonds. It's impossible to say anything about the structure...
Please explain how a) is solved, write what formula is used and explain in detail so I can solve any problem of this type. 2) Find the power and energy of the following signals (20 Points). a) x(t) = sin(t) b) y[n] = (-0.3)”u[n – 2] Solutions: Part (a): The signal r(t) is periodic because 1-cos(2t) (t) = sin(t) = ? Therefore, E = 0. To find the power, we can use the fact that the signal is sinusoid: P:...
The answer is c, Could you please explain in detail why The answer for this is d The answer is b, but d makes more sense to me Anwer is d /25. The formate anion, HCO, has delocalized electrons that populate three-centre n molecular orbitals similar to those of ozone. Assuming a ground state electron configuration, which of the following best represents the electron populations in these delocalized orbitals for the fomate anion? a. b. d. 元事 - 元* 元*...
please in as MUCH detail explain why this is the answer. what are pre and post trans/transl. and ALSO please explain what A through D are (definition and what it refers to in genetics) 37. Genetic regulation in eukaryotes can take place at a variety of levels from pre- transcriptional to posttranslational. At what level is genetic regulation considered most likely in prokaryotes? A) polyadenylation of the 3' end of the mRNAs B) capping ranscriptional D) intron processing E) exon...