2. (a) Starting with Propanol (CH3CH₂CH₂OH), show how would you synthesize the following substances? Use equations only, showing structures of reactants, reagents and all intermediate products. 6 (1) 3-Hexanol CH3CH₂CH₂(OH)CHCH₂CH3} (ii) Propanoic acid (CH3CH₂COOH) (iii) 2-Pentene (CH₂CH₂CH=CHCH3) (iv) Ethyl propyl ether (CH3CH₂CH₂OCH₂CH3) Y CH₂CH₂ CH₂CH₂CH₂ R-U-R ol when synthesizing = alcohol R-OH

(ii) Name the following using IUPAC system of nomenclature:   (a) CH2 (Cl) CH (NH2) CHO       (b) CH3 C (Br) CH2 CH (F) COOH                            Br

2, vi, viii, ix only those

Parts A,B&C Please.

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1d

Q2. Consider the nucleophilic substitution reaction between 3-chloro-3-methylpentane and the hydroxide ion: CI x + OH (a) Is the alkyl halide 1°, 2° or 3°? (b) Will the nucleophilic substitution reaction be S₁1 or S№2? (c) Give the substitution mechanism showing all full and partial positive and negative charges, electron movements using curved arrows.

Can i get help with this problem

1a）Give structures for the following compounds: a) phenyl isobutyl ether b) ethyl 4-phenylbenzoate c) 3-sec- butylpyridine d) 3-fluoro-3-hexen-2-one

Show how each alcohol or diol can be prepared from an alkene.(a) 2-Pentanol (b) 1-Pentanol (c) 2-Methyl-2-pentanol(d) 2-Methyl-2-butanol (e) 3-Pentanol (f) 3-Ethyl-3-pentanol(g) 1,2-Hexanedio