please explain how you get the answers especially for the multiplicity. Thanks in advance. 2. For...
2. For each of the following compounds, label hydrogens in equivalent environments, indicate the integration value and multiplicity for each signal а. b. с.
Please explain how did you get it Thanks in advance The figure is a snapshot graph of a sin wave at t=1.0 s. Draw a history graph of the point a x=1.5 m.
Please explain all steps. Include degrees of unsaturation, functional groups, and signals used to determine structure. For the compounds listed below: 1. (18 points) Label each set of chemically equivalent protons, using a for the set that will be have the lowest frequency (most upfield) in the 1H NMR spectrum, b for the next a. lowest, and so on. of each set of the equivalent protons. expected for each compound. b. Indicate the splitting pattern (singlet, doublet, triplet...) for expected...
I need help with all three parts. Can you please explain to me how do I calculate J values? 3) What is the structure of the compound in the following 1H-NMR spectrum with the molecular formula C2H, NO and a characteristic IR stretch near 1700 cm-1? Relative integration is shown. a) Explain the multiplicity and the chemical shift of each signal b) Indicate in each signal how you would calculate the coupling constants (). Give an approximate value (range) for...
Please explain how you get to the answers! Thanks 1. A mass is attached to a horizontal spring, and oscillates with a period of 1.2 s and with an amplitude o 12 c Att-0s, the mass is 6 em to the left of the equilibrium position, and moving to the right a) On the plot of the cosine function below, label the two points that could correspond to the phase offset if you consider just the initial psition of the...
need help understanding how to do this worksheet, please explain. thanks so much in advance 1. Classify the following compounds as a primary, secondary or tertiary amine mo o com 2. What is the IUPAC name for the following compound? many way as they 3. Arrange the following compounds in decreasing (strongest to weakest) order of basicit NH, O, NH, BH 128-
Please show work on how to get the answers. Thanks in advance! :) 7. Let P(-3,1)and Q(5.6) be two points in the coordinate plane. (a) Find the distance between P and Q (b) Find the midpoint of the segment Po. (c) Find the slope of the line that contains P and Q d) Find an equation of the line in standard form that contains P and 0 (e) Find an equation of the line in standard form that is perpendicular...
Could you do both questions? Thank you in advance! 2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism OK + E b. Redraw the product(s) below and label all the non-equivalent carbons. How many signals would you expect to see in the 13C NMR of the product? Predict the chemical shifts of each carbon below. c. Redraw the product(s) below and label all the non-equivalent hydrogens. How many signals would you expect to see...
could you all please show the answers to number 3, and show the answer and explain for number 5? answer to number 4 is not needed. please also draw out the spectrums for number 5. 3. What is the ratio of the protons for the following compounds (from left to right)? Provide multiplicity (splitting) for each proton. Provide number of different (symmetrically inequivalent) carbons for each compound. 3:2:3 Which compounds should have diastereotopic hydrogens? More than one correct answer is...
how would you get from the reactant to the product? thanks in advance! Synthesis Puzzle