Name the ¹H spin systems of the following compounds using Pople coupling nomenclature: A,B,M,X... Hint: Draw missing H-atoms first (A) OO (B) D₂N. (C) (D) 0 OD N ZO ND g OD
Q: Consider this ligand substitution mechanism where the three main paths are equally likely to occur…
A: Option 1: The percent of trans product isomer that forms will be at least 50%.Trans Products:Path A:…
Q: Bonus 2: What is the major product formed in the following reaction? H Br H CH3 NaOC(CH3)3 H3CH2C D…
A: Step 2: Step 3: Step 4:
Q: Help me with understanding this.
A: Step 1: ReactionClaisen rearrangement observed in Allyl Aryl ether give ortho Allyl phenol as major…
Q: Draw a mechanism for the formation of 4-methylcyclohexene by the dehydration of 2-methylcyclohexano.…
A: Step 1: Step 2: Step 3: Step 4:
Q: Please find the Rf values of each drug and the name of the unknown sample!
A: Step 1:1. TLC is used for various applications in organic chemistry, such as: a. Examining if two…
Q: Please correct answer and don't use hand rating
A: Let's go through this problem step by step: 1. Price Calculation when p2 = 13The consumer located at…
Q: Help me with my study guide
A:
Q: Please correct answer and don't use hand raiting
A: (a) 2,3-Dimethyl-2,3-butanediol1. Identify the longest carbon chain- The main chain has four…
Q: Please correct answer and don't used hand raiting
A: 2-methyl-1-butene:In this molecule, the vinylic hydrogens are attached to the carbons of the double…
Q: ropose a sequence of reactions to accomplish the following synthesis. O 1. Br2, light; 2. KOtBu;…
A: Step 1:Alkanes treated with Br2/hv to more more substitutes alkyl bromide Alkyl bromide with bulkier…
Q: Please correct answer and don't used hand raiting
A: Step 1: Step 2: Step 3: Step 4:Step 1) Methylbutanoate react with methylmagnesiumbromide form…
Q: Show work and with explanation needed...don't give Ai generated solution
A:
Q: 5. The alkylation of 1,4-dimethoxybenzene is shown below. OCH3 OCH3 C(CH3)3 18 M H2SO4 + (CH3)3 COH…
A:
Q: Give correct solution. don't give Ai generated solution
A: Step 1:To separate ethyl 4-hydroxybenzoate from 2-chloroacetanilide, a base extraction method is…
Q: Give detailed mechanism Solution with explanation needed. Don't give Ai generated solution. avoid…
A: LDA is a strong base and the hydrogen Alpha to the carbonyl group is acidic hydrogen. So at first…
Q: For the experiment of Investigating Entropy Trail 1: NaNO3: 4.288g, H2O: 50.605mL, inital…
A:
Q: of 25 > © Macmillan Learning Match each structure and description to the appropriate amino acid. لا…
A: Before we start matching, let's understand the terms. Amino acids are organic compounds composed of…
Q: Coul I have assistance for this mechanism? I am supposed to show the mechanism for the product! My…
A:
Q: For each pair below: a) Highlight the most acidic hydrogen in each molecule b) Draw the conjugate…
A: Step 1: Step 2: Step 3: Step 4:
Q: Calculate the solute mass required to prepare 100. mL of 1.0 M "table sugar" (sucrose C12H22O11)
A: The problem is asking for the mass of sucrose (C12H22O11) needed to prepare a 1.0 M solution in 100…
Q: Question 2 (this should take you no more than 10 minutes) (a) Identify significant regions of…
A:
Q: 2. The following compound is used to treat lung carcinomas. The drug inhibits a kinase by forming a…
A: Step 1:(a) The warhead is circled in the given molecule as shown below. The warhead is an…
Q: Please correct answer and don't used hand raiting
A:
Q: Give me detailed Solution. don't give Ai generated solution
A: The buffer solution is made of weak acid and its conjugate base, HBrO (acid) and BrO- (base). Buffer…
Q: Since silicates are polymers of the anion (SiO4)4-, it can be stated thata) the polyanions will have…
A: Anions are atoms or groups of atoms that have gained electrons. Because they now have more electrons…
Q: Please correct answer and don't use hand raiting
A: Step 1: Step 2: Step 3: Step 4:
Q: Show work with explanation... Don't give Ai generated solution
A:
Q: Which of the following alkyl bromides would undergo a relatively fast E2-type elimination reaction?…
A: Approach to solving the question:As we know, in E2 elimination, the rate of the elimination depends…
Q: (a) Construct a molecular-orbital energy-level diagram for N2. (b) Draw a лu2px molecular orbital. น…
A:
Q: Draw the major products of this organic reaction #20
A: Approach to solving the question: The given reaction is the hydrolysis of tertiary alkyl bromide in…
Q: For the following reaction, select all the statements that are correct. Br2 ? 1 Br Br Br Br Br Br Br…
A: Step 1: Br2 can react with unsaturated double bond which are not involved in aromaticity to form…
Q: I said don't use Ai only solve accurate. Chemistry expert only . suggest to Chemistry experts okk.…
A:
Q: Classify as aromatic, non-aromatic and antiaromatic: -N OH 8 OH b) S c) d) N: f)
A: a) Phenol (C6H5OH) - This is an aromatic compound with a benzene ring and a hydroxyl group. b)…
Q: Infrared Spectroscopy (IR) is very useful for determining the functional groups present in an…
A: Step 1: Identifying Functional GroupsFrom the IR spectrum -O-H group: Broad absorption around…
Q: jay.1
A:
Q: 1. Below is a molecular orbital diagram for a generic metallocene. Based on this, contrast the metal…
A: Here's a detailed interpretation of the molecular orbital diagram and analysis of the metal-carbon…
Q: Answer in step by step with explanation.
A:
Q: Knowing that the rotational constant B is 1.707 cm-1. Calculate the frequency of the transition J =…
A: To calculate the frequency of the rotational transition J=4←3 for the compound AB, we use the energy…
Q: W Wikipedia er 10 Ho... M Quiz for Ch 10... XM Question 24 of... f Facebook Twitter in LinkedIn Mail…
A:
Q: Please correct answer and don't use hand rating
A: Question 1: F2OStep 1: Calculate the total number of valence electronstotal=2×vF+1×vO=(2)(7)+6=20…
Q: Give detailed Solution with explanation needed....don't give Ai generated solution
A: Approach to solving the question: The given alkyl halide is tertiary alkyl halide which gives alkene…
Q: Section 2: Alkene Stability For each pair of alkenes, circle/indicate the most stable structure. F3C…
A: Step 1:Step 2: Step 3: Step 4:
Q: Question 1 (this should take you no more than 10 minutes) Explain how the charge distribution of a…
A: Here's a detailed explanation for each intermolecular force and how it is related to charge…
Q: Give me detailed Solution with explanation needed....don't give Ai generated solution
A:
Q: Please correct answer and don't use hand rating
A: Step 1:Identify the functional group and substituent s Functional group is cycloalkane Cyclic…
Q: Give complete reaction equations that show all intermediates, reagents and product if (R) -3-…
A:
Q: please draw each structure a, b, c, and d, e
A: Step 1: Step 2: Step 3: Step 4:
Q: Show work. don't give Ai generated solution
A:
Q: Please correct answer and don't used hand raiting
A: In figure we can see that the height if mercury column is larger in open end and smaller in gas end…
Q: what alkene has at least 8 carbons, more than one double bond, and has at least one oxygen (ether)…
A:
Step by step
Solved in 2 steps
- Cisplatin (cis-diamminedichloroplatinum(II)) is the first platinum-based antitumor agent, and it is still widely used in chemotherapy, whereas the trans isomer is therapeutically inactive. NH, H,N CI A Pt Pt CI NH3 CI NH, cis trans (cisplatin) a) Assign point group to A and B. b) Is it possible to distinguish A and B based on the Pt-Cl stretching vibrations using IR and/or Raman spectroscopic data? If so, explain how you could distinguish them using group theory.Identify w hich of the follow ing molecules are infrared active: N2, CO2, OCS, H2O, CH2 = CH2, C6H6.Giventhefollowingsetofreactionsandtheirenthalpies,drawtheBorn-Habercyclefortheformationof LiCl(s)anddeterminethelatticeenergyforLiCl.Reactions:H (in kJ)(1)Li(s)Li(g);Hs= 161;(2) Li(g)Li+(g)+e–;IE= 520;(3) ½Cl2(g)Cl(g);½BE =121.5;(4)Cl(g)+ e–Cl–(g);EA= –349;(5)Li+(g)+ Cl–(g)LiCl(s);UL= ?(UL= latticeenergy)(6) Li(s)+ ½ Cl2(g)LiCl(s);Hof=–408.6._______________________________________________________________________________
- Q2 a) Calculate the CFSE for the following ions in an octahedral field: Cr2+, Co2+, Mn2+ and Zn2+ ? b) Draw out the splitting of d orbital diagrams for the following: i) ML4 square planar. ii) Four long & two shorts tetragonal distortion.1) a) When CO becomes coordinated to BH3, its stretching frequency increases, but when CO is coordinated to Ni(CO)3, its stretching frequency decreases. Explain. b) Does the stretching frequency of CO increase of decrease when (explain too) i) L of L M-CO becomes more electron withdrawing. ii) CO of L₁M-CO becomes coordinated to a Lewis acid, A, to become LM-CO-A 18Determine the number (and relative intensity) of IR-active C–O stretching vibrations for fac-[Mo(CO)3(NCMe)3]: Proceed as follows... Determine the point group of the molecule. Do not descend in symmetry. Construct a reducible representation for the CO vibrations (ΓCO) -- [please explain how to determine the number of unshifted atoms] Decompose ΓCO into its irreducible representation ΓCO,i.r. Determine which are IR active (number of IR active modes) Double degenerate modes (i.r. with E symmetry) are ≈ twice as intense as other modes, and triply degenerate modes (i.r. with T symmetry) are ≈ three times as intense.
- What is the order of infra red stretching frequencies of the given compounds?(in increasing order)9. Consider the ethyl iodide molecule, CH CH₂, which of the statements below is correct? (A) CH, protons are more deshielded. (B) The energy gap between a and ß spin states of CH₂ protons is smaller than the counterpart of CH; protons. (C) The electronegative element I shields the CH₂ protons. (D) None of the above.12. Without performing any calculations, identify which stretching vibration will have the higher frequency in each of the following pairs. Explain. (a) C-O vs. C=O (b) H-Cl vs. H-Br
- Hh.213.3) The structure of 1,1,2,2-tetraiododisilane is shown below. Determine its point group. Predict the number of IR-active and Raman-active Si-I stretching vibrations for each molecule. H. Si H.The absorption pattern in the UV/VIS region corresponds to (a) bond vibrations b) valance electron transitions =) molecular rotations E) nuclear spin 0000 a an IR spectrum