| ¿µ¹® | isomer | ÇÑ±Û | À̼ºÁúü, À̼ºÃ¼ |
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| ¼³¸í | 1. °°Àº ¿øÀÚ ¹øÈ£¿Í Áú·®¼ö¸¦ °¡Áö¸é¼ ¹Ý°¨±â, ¿¡³ÊÁö »óÅÂ, ¹æ»ç´ÉÀÇ ¼ºÁúÀÌ ´Ù¸¥ ¿øÀÚÇÙ. 2. ºÐÀÚ½ÄÀº °°Áö¸¸ ´Ù¸¥ ¹°¸®Àû-ÈÇÐÀû ¼ºÁúÀ» °®´Â ÈÇÕ¹°. ºÐÀÚ ¾È¿¡¼ ¿øÀÚÀÇ ¹è¿ ¹æ½ÄÀÌ ´Ù¸£±â ¶§¹®¿¡ ÀÌ·¯ÇÑ ÈÇÕ¹°ÀÌ »ý±ä´Ù. |
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| DL | danger list; De Lee [catheter]; deep lobe; developmental level; difference limen; diffusion lung [ca... |
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| levorotatory isomer | A stereoisomer that rotates the plane of polarized light counterclockwise. (09 Oct 1997) |
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| levorotatory | <chemistry> A chiral molecule which rotates plane-polarized light to the left. (09 Jan 1998) |
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| geometric isomer | <chemistry> Geometric or also called cis-trans isomers are stereoisomers in molecules with restricted rotation about a bond. Cycloalkanes and alkenes form cis-trans isomers due to the restriction of rotation about the double bond or due to the restriction in a ring. In order for an alkene to freely rotate, the pi bond must be broken. This process has a high activation energy and does not occur at room temperature. Cis isomers have the two substituents on each of the carbons of the double bond on the same side, whereas in the trans isomer they are on opposite sides. The expression cis and trans only applies to alkenes or cycloalkanes if one of the substituents on each of the carbons are the same. If there are three or four different substituents, E,Z or R,S nomenclature must be used. (09 Jan 1998) |
| chain isomer | <chemistry> One of two or more compounds having the same chemical composition but differing in the arrangement of the atoms (usually carbon atoms) forming the backbone of the structure of the compounds. (21 Mar 1998) |
| dextrorotatory isomer | A stereoisomer that does a clockwise rotation of plane-polarized light. (09 Oct 1997) |
| isomer | 1. <chemistry> One of two or more molecules that have the same chemical formula but have a different stereochemical arrangement of their atoms. 2. <radiobiology> Nuclides having the same number of neutrons and protons but capable of existing, for a measurable time, in different quantum states with different energies and radioactive properties. Commonly, the isomer of higher energy decays to one of lower energy by the process of isomeric transition. (13 Nov 1997) |
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