Qa) Show the possible stereoisomers of octahedral (Re(NH3)2(x)] HT namleves would exhibit optica
b) Sketch all possible geometrical isomers and then indicate which of these complexes would exhibit optica activity. Also identify each complex by name a) [Fe(C,0.).cllion (C.0, oxalate ion), b) [PdCI,(PP) Q4. Assigne the point group of the following compounds (show all your work)
in question 3, are they asking for the stereoisomers ? which would be six possible stereoisomers ? If so then no need to answer question 3. Thanks. sorry, i meant question 2. 2. Draw all possible isomers of the following compound and assign all of the hydrogen atoms on each carbon atopm (except for methyl hydrogens) as homotopic, enantiotopic or distereotopic. 3. Estimate the ky/kp values for the following reactions and explain your reasoning. what can you be HCN H...
A) how many stereoisomers are possible for this compound? Show how this can be easily determined mathematically B) draw all stereoisomers for this compound. Use dashes and wedges appropriately at each stereo center. DO NOT SHOW HYDROGEN ATOMS @ EACH STEREOCENTER C) Identify and label each pair of stereoisomers drawn in part B (above) as either enantiomers or diastereomers D) identify and label each pair(s) of stereoisomers that would be optically inactive as 50/50 mixture in a polarimeter and explain...
2. a. Draw and show the crystal field splitting of the d orbitals in an octahedral complex, a tetrahedral complex, and in a square planar complex.(clearly label the orbitals) b. Explain the difference in the following crystal field splitting values (1) Co(NH3).]2+ 10200 cm"! : [CO(NH3).]* 22,900 cm (ii) [Cr(H20).]** 17,400 cm. ; [Cr(CN).]3-26,600 cm (iii) [MnF6]?- 22,200 cm-"; [ReF.]?- 27,800 cm- (iv) [Co(NH3).]2+ 10,200 cm '; [Co(NH3)4]2+ 5,900 cm c. Draw and show the filling of 6 d electrons...
2) a) Consider 2-bromo-3-chlorobutane. How many stereoisomers are possible for this compound? Draw all stereoisomers, label each stereocenter with the appropriate R/S designation to show handedness, and indicate the relationship (enantiomers or diastereomers) between every possible pairing of compounds. Name each compound according to IUPAC nomenclature, using appropriate R/S designation to show handedness. b) Repeat this exercise for 2,3-Butanediol. What is different about this compound relative to the first example? What word describes the unique stereoisomer? c) Which of the...
predict the product(s) which would be expected. if multiple stereoisomers are possible draw all of them. Br Br Br Br 1) xs NaNH2 2 H₂O Br
1. [Mn(H2O)6]2* Draw the possible stereoisomers. Give the oxidation state of the metal. Identify the donor atoms. Draw the structure of the transition metal complex ion. Show the charge on the complex. Determine if its paramagnetic. State whether the complex is high-spin or low-spin. Draw the ground state arrangement of the d-electrons. Calculate the LFSE (in units of A or AT) for each complex.
physical chemistry, please show all work and explanations clearly 2. For the gas-phase reaction 2 NH3 <=> N2 + 3 H2, a closed system initially contained 1.00 mol of NH3, 4.50 mol of N2, and 4.20 mol of H2. Once equilibrium is achieved a) what are the minimum and maximum possible values for £? [-1.40 s E s 0.50] b) what are the minimum and maximum possible values for nNH,, NN,, and nu,?
2. For a discrete random variable X, with CDF F(X), it is possible to show that P(a < X S b)-F(b) - F(a), for a 3 b. This is a useful fact for finding the probabil- ity that a random variable falls within a certain range. In particular, let X be a random variable with pmf p( 2 tor c-1,2 a. Find the CDF of X b. Find P(X X 5). c. Find P(X> 4). 3. Let X be a...
2. Show that each of the following utility functions has a diminishing MRS. Do they exhibit constant, increasing, or decreasing marginal utility? Is the shape of the marginal utility function an indicator of the convexity of indifference curve? a. (2) U(X,Y) = XY b. (2) U(X,Y) = x2y2 c. (2) U(X,Y) = In X + In Y