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- Functional Groups - Halogens, Alcohols & Ethers Functional Groups Besides hydrogen or carbon bonded to carbon Many other atoms can bond to carbon and these Lead to the formation of what are called “Functional groups” Each Functional group has it’s own unique chemical And physical properties So what kind of functional groups are there? Check out Table R in your Reference Table. TABLE R – Functional Groups -Halides -Alcohols -Ethers Organic Halides • One or more of the hydrogen atoms in an alkane is replaced with a halogen – F, Cl, Br, or I • Not hydrocarbons! Often called halocarbons. Properties of Alkyl Halides Alkyl halides are extremely unreactive Often used when chemical inertness is important -Examples: CFC’s (refrigerants, Aerosol propellants, Teflon (polymer), Brominated compounds (Fire retardant clothing) -many of these compounds are now banned from use for health and environmental reasons. Properties of Alkyl Halides Alkyl halides due to there high molecular wt. have considerably higher B.P. than their corresponding alkanes Propane Chloropropane Bromopropane B.P. (deg. C) -42 47 71 Density (g/ml) (Gas) .890 1.335 Bonds are polar but compounds are not soluble in water Probably because they can’t form H bonds Is CHCl3 a polar compound? Yes What about CCl4? No Naming Organic Halides Use prefixes to specify substituent: – fluoro, chloro, bromo, iodo • If more than one, use di, tri, etc. to specify # of substituents. • If necessary, give locations by numbering C-atoms in backbone so that the halide has the lowest number. c-c-c-c-c Br Br 2,3-dibromopentane Naming Halides CH3Cl CH3CHFCH3 H H–C–Cl H H H H H–C–C–C–H H F H Chloromethane “Chloroform” 2-fluoropropane C3H7F Name the following Compound: CH3CCl2CHClCH3 H Cl H H H–C–C–C–C–H H Cl Cl H 2,2,3-trichlorobutane C4H7Cl3 Name this compound: 3-Bromo-2-Iodopentane Name this compound: F H-C F Cl 1,1-dicloro-2,2-difluoroethane Cl One of the “freons” C-H Alcohols • Alcohols contain the polar -OH functional group – OH groups are capable of Hydrogen bonding • This polar functional group affects physical properties – B.P is much higher than the corresponding Alkane • Ethanol (C2H5OH) +78C // Ethane (C2H6) -89C – Low Mol. Wt. Alcohols are very soluble in water Hydroxyl groups Alcohols can hydrogen bond because they have a Hydrogen atom that is bonded to oxygen. This results in Much higher B.P.’s And higher water solubulity CH3–CH2–O-H CH3–CH2–O-H H-O-H Physical properties of Alcohols Name Formula B.P. (C) Sol. (g/100g H20) Methanol CH3OH 64.5 Fully miscible Ethanol CH3CH2OH 78.3 Fully miscible Propanol CH3(CH2)2OH 97 Fully miscible Butanol CH3(CH2)3OH 118 7.9 Naming Alcohols • Select as the parent structure the longest continuous carbon chain that contains the –OH • Drop the –e from the alkane name of the carbon chain and add –ol • Indicate by a number (if necessary) the position of the –OH group ethanol 2-propanol Types of Alcohols Alcohols are also considered to be either - primary, secondary, or tertiary alcohols Designations correspond to which carbon atom the –OH group is bonded to - Affects Chemical Reactivity/Properties - Tertiary more reactive than Primary Primary alcohol: Secondary alcohol: Tertiary alcohol: OH bonded to –CH20H OH bonded to –CHOH OH bonded to -COH Types of Alcohols Primary alcohol Secondary Alcohol Tertiary Alcohol Ethers Even though ethers have an oxygen atom in their Structure they are unable to form hydrgen bonds with themselves - alkyl groups are bonded directly to Oxygen - No hydrogen bonded to Oxygen Ethers are not linear; They have a bent shape similar to water Ether’s Properties BP’s tend to be low Comparable to similar MW hydrocarbons No internal H-bonding Solubility in water is reasonably high for lower M.W. ethers H-Bonding to Water is possible Propane Dimethylether Diethylether M.W. 44 46 74 B.P. (deg. C) -42 -24 35 Sol in Water (g/ml) Na Na 8 Naming Ethers (common names) • Name the groups (alkyl) on either side and add ether to the end. • List attached alkyl groups in order of increasing size • If they are the same the side chain is labeled “Di” • NO NUMBERS NEEDED to designate location of Oxygen! Naming Ethers Name this compound: Dimethyl ether Name this compound: Ethylpropyl ether