bate eG Turoqnt | cHM301 eeeennenee ee _—— Ss ___|Guestion_ | i 5 methyl - 2,44 ~ hexanedio! {2 methyl ~ +t =phenyl ~ 2-butanol :)4H- dimethyl cyclohexanol | 2-bromocyclapentano! _ ztans ~2 ~bromocyclopentano! 231 4 = bromo - 3-Methy| phenol '2- cyclopenten tot 5 nc Question 2 F he | Compound A: Ethanol = [compound B + 2-metiy!-2-propanol [ by] compound A : primary aleshol compound 8 : Tertiary alcoho! HH CHa ' H=9-G ~OH ca, Ot = HH ‘ - Cs Question 3 + m i)_1 = pentanel + pinay, alcohol 7 to I Ys ‘OH [in 2,2, -trimethylpentan-3-01 Tertiary alcohol : = | ou! on 7 1 Gs | Matis 1 Cy | Cis Wi) 4, H-dimethylpentan -2-0! > Secondary alecho) | excel pe | ae ‘OH \—Usi Scanned with CamScannerPimary alcohol > secondary alcohol > tera alcoho! _b ag ne a tere [Bolling points smcrease as the number of carbone. Increased. “Boneh Increase 2! derlpry. alcohol — — - —__Strondoty_ 4.-qlcohol ei lob nee 01 + primary alephol 1 Scanned with CamScannertate is ah Date: e the ff ous g \ Brchloro = 3-€thyl phenol 4-heptene - 2-ol : x ci é | oO AAS : sxondary algohol secondary alcohol w= Primer aleshol ,cecondary aleshol_and tertiary alcehol q = 9 ao Question 6 - ay*t -phenyl_~ 2- pentanol by] [+3 -propanedial butan-t-ol HO OH ow FAI alcobels can form_injermolecular_hydrogen_bonding but diols have more oppurtanity fo form _hydrogen_bonds becauce_of wo oH groups A Tnisamolecular hydrogen bonds leads 10 reduced boiling points. ¥ Bulon-1-0l <_!,3 propanedio! ~ | Question 7 a)| Compound _A_: 3-cyclopenty! “ethanol 2-oy lopenty| ethanol Compound B + 3-methyl 72-nitrophenol 4 -methyl ~ 3 -witro plnen ol by | Compound C > compound D > compound © Compound © > compound D> compound C Bimary hae avtergert largest boiling pert CS Scanned with CamScannerNo. Date . 1 Sue $ | Alcohol A: 3“‘brame ~ 4-penten -9-o1 Alcohol B = 3>qinino -4-nirophenol | } Guewion & @ 2 B-pentanol ic a secondary alcohol while 3-methy!-3-pentanol_is_o kerhary alcohol *3-penianol will appear as clear solution after 6 minutes while for 3-methy/ Hydroxy|_/-oh lucas {est : 3"pentanol , ct will form cloudy dispersion er separated layer immediatel by | Todoform tes! (Ethanol _bagi respond) i “Ethano] wil form poke yellow predpitate while bo changes observed for |- propanol r . i Tt Scanned with CamScanner