Question

PART A: Table 10.1 Hydrocarbons Organic Compound Structural Formula Draw as type A) Type of Hydrocarbon Name of Compound (IUPAC name preferred CH CH, CH CH, (the alkene) CH, сн. (the alkyne) CH,CH,CH, (the aromatic)

Answer 1

Hydrocarbons Organic compound structural Ja formula Types of hydrocarbon name of compound (IVPAC name) ethane C2H6 H3C- CH3 Alkone C3H8 CH3 -CH2-CH3 Alkane Propane C2H4 I HQC = Chef Alkene ethene C3H6 MC-CH=CHR. Alkene Prop-l-ene C2H2 H-CEC- Alkyne Ethyne (3H4 HC EC-CH3 Alkyne propyne CGHSCHOCH3 C H2-CH3 Aromatic 1-ethyl bemene Organic compound structured formula Hychocoroton derivative. Name of Compound (IUPAC Name)

organic compound structural formula Hydrocarbon derivative Name op.comp. (IUPAC name) CH3CH2C1 HC-CH2-C1 | Alkyl holide chloroethane C6H5Br er Aromatic I halide - bromo benzene CH2CH.COH)CH2CH3 CH3 - CH-CH2-CH3 Alcohol OH 2-hydroxy butane OH Alcohol C6H4CCH3) com, p) Draw three isomer 2-methylbenzeno) (o-methyl phenol) 3-methylbenzenol (m-methyl phenol) 4-methylbenzeno (p-methyl phenol) CH3 CH3CH2CH3 HF-CH2-0-CH3 Ether methoxy ethane CH3NH2 H3C-NH2 Amine Methanamine MH2CH2COOH How-CH2-C-om Amino acid 2-aminoethanol excid. CH3 CHA CHO i ISH3-cu CH3-CH2-C- H I Aldehyde Propanal - CH2CH2 COCH2CH2CH2CH2-C-CH2-Chla Ketone Pentane-3-one t Acid Propanoic acid CH3CH2Cool CH3-CH2-COM CHACONHA CH2 - CHINHO cuacha Cooch3 CH3-He- Locke C.HSCONH2 CH3-CH NH2 Amide Ethanamide ester + methylpropanoole

Organic.comp. IUPAC nume. Common Name Me Be Density CH2COOH ethanoic acid Acetic acidi 16.6 118 16044 Propane-2-one Acetone -94.7 56.05/0.7845 CGHG Benzene Benzerte 5.5 80.1 (0.8765 CH3COCH 3 CHC13 Trichloromethand chloroform -63.4_61.2 1.4788 CH3CH2OH Ethanol ethylacobel -114.1 78.5 0.789 CH3CHROCH2CH3 ethoxyethune diethyl ethey -116.2 345 0713 CH3600CH2CH3 ethyl ethanoate ethylacetate -83.6 77 0.895 CH3CHCOH) CH3 propune-2-61 Isopropyl alcobel – 88.5 82.4 0.785 Methanol Methyl alcohol -109. 55.2 CH3OH 0.741 CGHScH3 i-methyl benzend Tolune - 93 110.6/0.867 |

organic comp. Constitutional isome Name of isomea CH3-CH2-CH2-CH3 n-Butane C4H10 ist isomer 2-methyl propane C4H10 2nd isomer. CH3 -CH-CH3 CH CH3-CH2-CH2-CH2-CH3 n- pentane (SH12 st isomer CH3 -CH=CH2-CH3 2-methyl but one (5H12 and isomer ! CHS 2,2-dimethylpropane (5H12 3rd isomer H3C-C-CH3 CH3 Organic compound Draw the come (type B) CH2B71 Mimor image of comp 1 (mark any chiral centers) BEC-I ItuI

organic compound - CHCIBRE Draw the comp (type B) (mark any chiral center mimmy image of comp (Mark any chiral center) C- H The compound is a chiral. It has a four different 20up attached on a carbon which is stereogenic Corrbon. The mimor images of the CH2 Br I is non super- imposable if they are not mimor images to each others. The compound consist of a stereogenic center they che active and they have non superimposable mimor images to each other. Therefore they are enantiomers

Organic compound Alkene isomers. Name of the isomer (type A) | Using als strans c=6 BYHC=CHBO ist isomer Br Br (is isomer Isimilar group on L same side BcHC ECHBT 2nd isomer trans isomer I similar proup on Lopposite side CH3CHECHCH2CH2013 ist isomer CH2CH2CH3 Cis isomer [Higher priority qoup on sume side CH2CH2CH3 CH3CH2CH CH2CH2CHB and isomer trans isumer [Higher priority group on opposite Side]

Organic compound Name of each of the isomer using the E, z system isomer Br C=C st isomer E isomer -=6 He 2nd isomer Bel CH2 CH2 CH3 Isomer ele2 ist isomer E isomer - CH2CH2CH3 The higher priority group on the same side The compound is suid that I isomer' & The higher priority group on the oppossite side. The compound is said 'G' isomer