The given ball and stick model of estragole to a skeletal structure has to be drawn and functional groups has to be identified. Concept Introduction: Skeletal structures Skeletal structures are used for representing the organic structures in diagrammatic form. The carbon atom must have four bonds. The heteroatom should not contain its lone pair of electrons. The double bond and triple bond has to be drawn. The hydrogen bonded directly to heteroatom has to be drawn. The carbon and hydrogen present in ring or chain compound has to be omitted. Functional group: Functional group contains particular atom or group of atoms bonded in a molecule which has specific chemical and physical properties. Adding any specific functional group to compound can form a new product it is known as functionalization. The functional group contains heteroatoms and a multiple bond in a compound.

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Chapter 10, Problem 10.60AP

Interpretation Introduction

Interpretation:

The given ball and stick model of estragole to a skeletal structure has to be drawn and functional groups has to be identified.

Concept Introduction:

Skeletal structures

Skeletal structures are used for representing the organic structures in diagrammatic form. The carbon atom must have four bonds. The heteroatom should not contain its lone pair of electrons. The double bond and triple bond has to be drawn. The hydrogen bonded directly to heteroatom has to be drawn. The carbon and hydrogen present in ring or chain compound has to be omitted.

Functional group:

Functional group contains particular atom or group of atoms bonded in a molecule which has specific chemical and physical properties. Adding any specific functional group to compound can form a new product it is known as functionalization. The functional group contains heteroatoms and a multiple bond in a compound.

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TRANSMITTANCE เบบ Please identify the one structure below that is consistent with the 'H NMR and IR spectra shown and draw its complete structure in the box below with the protons alphabetically labeled as shown in the NMR spectrum and label the IR bands, including sp³C-H and sp2C-H stretch, indicated by the arrows. D 4000 OH LOH H₂C CH3 OH H₂C OCH3 CH3 OH 3000 2000 1500 HAVENUMBERI-11 1000 LOCH3 Draw your structure below and label its equivalent protons according to the peak labeling that is used in the NMR spectrum in order to assign the peaks. Integrals indicate number of equivalent protons. Splitting patterns are: s=singlet, d=doublet, m-multiplet 8 3Hb s m 1Hd s 3Hf m 2Hcd 2Had 1He 鄙视 m 7 7 6 5 4 3 22 500 T 1 0