Concept explainers
Interpretation:
The reaction between trimethyl amine and
Concept Introduction:
▸ Lewis acids are electron pair acceptors.
▸ Lewis bases are electron pair donors.
▸ The valence shell electron pair repulsion (VSEPR) theory predicts the arrangement of atoms in molecules and ions.
▸
▸ They can act as nucleophiles and electrophiles in organic reactions.
▸ Amines can be classified into three categories: primary amines, secondary amines, and tertiary amines.
▸ If the nitrogen atom is directly attached to only one other carbon atom, the amine is a primary amine.
▸ If the nitrogen atom is directly attached to two other carbon atoms, the amine is a secondary amine.
▸ If the nitrogen atom is directly attached to three other carbon atoms, the amine is a tertiary amine.
▸ Higher the electron density around the nitrogen atom, more available is the electron pair to donate. Electron donors are Lewis bases.
▸ The reaction is Lewis acid- base reaction. The trimethyl amine donates a pair of electrons, so it acts as a Lewis base and
▸ Hybridization is the concept of mixing atomic orbitals into new hybrid orbitals which are suitable for pairing of electrons to form
▸ Hybrid orbitals are very useful in the explanation of molecular geometry.
▸ A trigonal planar geometry has
▸ A tetrahedral geometry has
▸ When one s-orbital and one p-orbital combine, it forms two
▸ When one s-orbital and two p-orbital combine, it forms three
▸ When one s-orbital and three p-orbital combine, it forms four
Want to see the full answer?
Check out a sample textbook solutionChapter 2 Solutions
Organic Chemistry
- There are two C–C single bonds in penta-1,3-diyne. (a) Which of those bonds would you expect to be stronger? (b) Which of those bonds would you expect to be shorter? (c) The molecule is moderately polar, with a dipole moment of 1.37 D. In which direction would you expect the dipole moment to point? Explain. Penta-1,3-diynearrow_forwardGive detailed Solution with explanation needed..don't give Handwritten answerarrow_forward(d) Compound W has the molecular formula C.H.O. Compound W reacts when heated with ethanoic acid and a catalyst to produce a sweet-smelling liquid. (i) Give the name of the homologous series to which compound W belongs. (ii) Draw the structure of compound W. Show all of the atoms and all of the bonds. SVENTarrow_forward
- Consider Lewis formulas A, B, and C:(a) Are A, B, and C constitutional isomers, or are they resonance contributors? (b) Which have a negatively charged carbon? (c) Which have a positively charged carbon? (d) Which have a positively charged nitrogen? (e) Which have a negatively charged nitrogen? (f) What is the net charge on each? (g) Which is a more stable structure, A or B? Why? (h) Which is a more stable structure, B or C? Why? (i) What is the CNN geometry in each according to VSEPR?arrow_forwardFor each of the following structures,1. Draw a Lewis structure; fill in any nonbonding electrons.2. Calculate the formal charge on each atom other than hydrogen.(a) CH3NO(nitromethane)(b) (CH3)3NO(trimethylamine oxide)(c) [N3]-(azide ion)(d) [(CH3)3O]+ (e) CH3NC (f) (CH3)4NBrarrow_forwardRizatriptan (trade name Maxalt) is a prescription drug used for the treatment of migraines. (a) How many aromatic rings does rizatriptan contain? (b) Determine the hybridization of each N atom. (c) In what type of orbital does the lone pair on each N reside? (d) Draw all the resonance structures for rizatriptan that contain only neutral atoms. (e) Draw all reasonable resonance structures for the five-membered ring that contains three N atoms.arrow_forward
- Rizatriptan (trade name Maxalt) is a prescription drug used for the treatment of migraines. (a) How many aromatic rings does rizatriptan contain? (b) Determine the hybridization of each N atom. (c) In what type of orbital does the lone pair on each N reside? (d) Draw all the resonance structures for rizatriptan that contain only neutral atoms. (e) Draw all reasonable resonance structures for the five-membered ring that contains three N atoms.arrow_forwardA1.arrow_forwardRizatriptan (trade name Maxalt) is a prescription drug used for the treatment of migraines. (a) How many aromatic rings does rizatriptan contain? (b) Determine the hybridization of each N atom. (c) In what type of orbital does the lone pair on each N reside? (d) Draw all the resonance structures for rizatriptan that contain only neutral atoms. (e) Draw all reasonableresonance structures for the ve-membered ring that contains three N atoms.arrow_forward
- Predict how the bond, shown in each of the following compounds will break with the aidof the appropriate arrow(s). Also give the structure(s) of the species formed in eachreaction.(a) CH3── I →(b) Q ── Q →arrow_forward(a)The concept of hybridization was first proposed by Linus Pauling in 1931, that explain about the concept of mixing orbitals to form new hybrid orbital suitable for the pairing of electrons to form chemical bonds. Draw the kekule structure of a compound that contains only carbon and hydrogen atoms that has: (1) One sp hybridize carbon, two sp? hybridized carbons and two sp hybridized carbon (ii) Two sp' hybridized carbon and two sp hybridized carbons (ii) Two sp? hybidized carbons and two sp hybydized carbonarrow_forwardWrite structural formulas for all the constitutionally isomeric compounds having the given molecular formula.(a) C4H10(b) C5H12(c) C2H4Cl2(d) C4H9Br(e) C3H9Narrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning