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

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Chapter 2 Solutions
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
- CH3CH2CH=CH2 + H₂O − H+arrow_forwardГ C-RSA CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.0 b.092 0.797 1.088 1.813 C-RSA CHROMATOPAC CH=1 Report No. =13 ** CALCULATION REPORT ** DATA=1: @CHRM1.000 11/03/05 08:09:52 CH PKNO TIME 1 2 0.797 3 1.088 4 1.813 AREA 1508566 4625442 2180060 HEIGHT 207739 701206 V 287554 V MK IDNO CONC NAME 18.1447 55.6339 26.2213 TOTAL 8314067 1196500 100 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0. 0 087 337. 0.841 1.150 C-R8A CHROMATOPAC CH=1 Report No. =14 DATA=1: @CHRM1.000 11/03/05 08:12:40 ** CALCULATION REPORT ** CH PKNO TIME AREA 1 3 0.841 1099933 41.15 4039778 HEIGHT MK IDNO 170372 649997¯¯¯ CONC NAME 21.4007 78.5993 TOTAL 5139711 820369 100 3 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.100 0:652 5.856 3 1.165 C-RSA CHROMATOPAC CH-1 Report No. =15 DATA=1: @CHRM1.000 11/03/05 08:15:26 ** CALCULATION REPORT ** CH PKNO TIME AREA HEIGHT MK IDNO CONC NAME 1 3 3 0.856 4 1.165 TOTAL 1253386 4838738 175481 708024 V 20.5739 79.4261 6092124…arrow_forwardIndicate the product that is obtained if the benzotriazole reacts with the use of a medium basic product.arrow_forward
- Indicate the product that is obtained if the benzotriazol reacts with dimethyl sulfate.arrow_forwardIndicate how to obtain 2-metilbencimidazol from 1,2-diaminobenzene.arrow_forwardbreak down both reactions shown and explain it correctly using the bromonium ion mechanism, instead of the (disproven) carbocation-based mechanism.arrow_forward
- Indicate how from 1,2-diaminobenzene to obtain 1-metilbenzotriazol.arrow_forward-C = C - C - + Br₂ + I" -> -C-C-c -C = C -C- + Br² + I₂ -C=C Br I + Brū + Iz -7- C - C-C- I Br Mechanism; - C = c - c - + Br - Br > - C-c-c- Br -C-C-C- + 1 - - -Ċ-Ċ'-c' - Br Br Iarrow_forwardWrite the mechanism of the esterification reaction (please show the mechanism included line pairs and arrows)arrow_forward
- How do I break down the reaction shown on the chalkboard and explain it correctly using the bromonium ion mechanism, instead of the (disproven) carbocation-based mechanismarrow_forward¿Qué the product is obtained from tetraethoxypropano and hidrazina?. Indicate the reason why the corresponding dial is used.arrow_forwardIf CH3COCH2CH(OCH3)2 is reacted with hydrazine, two isomeric products are formed. Indicate their structures and the major product.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
