3. Answer the following questions about the isomers fulminic acid(left) and isocyanic acid(right). H–C=N=0: H-C=N-0: a. A graph of potential energy versus internuclear distance for the C-N bond is isocyanic acid is given to the right. Sketch a curve that corresponds to potential energy versus internuclear distance for the C-N bond in fulminic acid on the graph. ir

3. Answer the following questions about the isomers fulminic acid(left) and isocyanic acid(right). H–C=N=0: H-C=N-0: a. A graph of potential energy versus internuclear distance for the C-N bond is isocyanic acid is given to the right. Sketch a curve that corresponds to potential energy versus internuclear distance for the C-N bond in fulminic acid on the graph. ir

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter17: Conjugation And Molecular Orbital (mo) Theory

Section: Chapter Questions

Problem 10E

See similar textbooks

Similar questions

Calculate deltaG in kJ NO2 (g) + SO2 (g) --> NO (g) + SO3 (g) deltaGo (NO2) = 51.37 kJ/mol deltaGo (SO2) = 81.98 kJ/mol deltaGo (NO) = -297.89 kJ/mol deltaGo (SO3) = -371.71 kJ/mol
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._______________________________________________________________________________
Rank the following acids in order of strength. H2S, CHCl3, H2Se, CH2Ch2
What is the configuration of the following compoound?
.For anion NO2-, (a) predict the stereochemistry. Justify your prediction with VSEPR theory and by formal charge; (b) indicate the hybridization appropriate to the stereochemistry; (c) describe the bond character of N-O for the resonance structure.
Most naturally occurring amino acids have chiral centers (the asymmetric a carbon atoms)that are named (S) by the Cahn–Ingold–Prelog convention (Section 5-3). The commonnaturally occurring form of cysteine has a chiral center that is named (R), however.(a) What is the relationship between (R)-cysteine and (S)-alanine? Do they have the oppositethree-dimensional configuration (as the names might suggest) or the same configuration?(b) (S)-Alanine is an l-amino acid (Figure 24-2). Is (R)-cysteine a d-amino acid or anl-amino acid?
For each of the following perrs what relationships exist between the two structures?
With link additivity values estimate DH ° 298 for CH3CH2OH (g) → CH3OCH3 (g).
What is the standard free energy change for the ionization of ethanolamine, if its kb is 3.20e-5.
1. Write the a) Lewis dot formula, b) line angle formula and of the following molecules: A. HCN B. NH3 2. What is the difference between homolysis vs. heterolysis. Show by giving an example.
Consider a d8 compound [like Pt(II)]. What is more likely to form a 4-coordinate or a 6-coordinate compound. Explain using VB theory and CFT. Good hand written explanation Asap
What kind of isomerisation occur in the pairs a-f?